Breast cancer metastases are most commonly found in bone, an indication of poor prognosis. Pathway-based biomarkers identification may help elucidate the cellular signature of breast cancer metastasis in bone, further characterizing the etiology and promoting new therapeutic approaches. We extracted gene expression profiles from mouse macrophages from the GEO dataset, GSE152795 using the GEO2R webtool. The differentially expressed genes (DEGs) were filtered by log2 fold-change with threshold 1.5 (FDR < 0.05). STRING database and Enrichr were used for GO-term analysis, miRNA and TF analysis associated with DEGs. Autodock Vienna was exploited to investigate interaction of anti-cancer drugs, Actinomycin-D and Adriamycin. Sensitivity and specificity of DEGs was assessed using receiver operating characteristic (ROC) analyses. A total of 61 DEGs, included 27 down-regulated and 34 up-regulated, were found to be significant in breast cancer bone metastasis. Major DEGs were associated with lipid metabolism and immunological response of tumor tissue. Crucial DEGs, Bcl3, ADGRG7, FABP4, VCAN, and IRF4 were regulated by miRNAs, miR-497, miR-574, miR-138 and TFs, CCDN1, STAT6, IRF8. Docking analysis showed that these genes possessed strong binding with the drugs. ROC analysis demonstrated Bcl3 is specific to metastasis. DEGs Bcl3, ADGRG7, FABP4, IRF4, their regulating miRNAs and TFs have strong impact on proliferation and metastasis of breast cancer in bone tissues. In conclusion, present study revealed that DEGs are directly involved in of breast tumor metastasis in bone tissues. Identified genes, miRNAs, and TFs can be possible drug targets that may be used for the therapeutics. However, further experimental validation is necessary.
Worldwide, breast cancer is known to contribute to the highest incidence of cancer-related mortality in women . Metastatic recurrence in breast cancer is associated with poor prognosis and is a leading cause of cancer related death in women worldwide . Despite improved treatments and surgical interventions, about 30% of patients lose their life due to metastasis .
Among metastasis in several other tissues and organs in the body (lungs, liver and brain, in addition to lymph nodes), bone is one of the most common sites of invasion in breast cancer [1, 4]. Metastasis to bone typically results in a poor prognosis, reducing life expectancy to 2–3 years post-diagnosis. The tumor cell mass exerts mechanical pressure that can contribute to bone pain. Pain may also occur due to release of inflammatory cytokines from the tumor cells themselves or by altering the bone microenvironment and bone homeostasis in adjacent areas .
Bone cancer metastases usually occur in the axial skeleton, in areas with active hematopoiesis and high red marrow content. The microenvironment is fundamental in attracting tumor cells to the bone as well as promoting tumor progression. The composition of the tumor microenvironment changes during tumor development, evolving to meet the demands of the growing neoplasm . These differences affect the progression of cancer and how it responds to therapeutic agents and their ultimate efficacy. An elaborate network of signaling pathways orchestrates the communication between cancer cells and the surrounding stroma. Chemotherapy, radiation therapy, and surgical removal of the tumors are standard methods implemented to cure breast cancers. The usage of thermoset based polymers [7–9] as a drug delivery system is currently a common approach when exploring chemotherapy as an option . Several chemotherapeutic molecules have proven their potential in treatment of breast tumour. Actinomycin D and its analogues and Adriamycin (aka doxorubicin) have been shown to reduce the migration and invasion of tumour cells [11, 12].
In this study, we explore different signaling pathways and associated molecular mechanisms of underlying primary breast cancer development, along with the formation of metastases in the bone. The study will also illustrate biomarkers associated with disease pathophysiology and highlight potential new therapeutics.
The expression profile information of mouse macrophages was extracted from the GEO dataset, GSE152795 (https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE152795). The annotation was performed using Affymetrix GeneChip® Mouse Gene 2.0ST Array. The dataset included breast cancer bone metastasis in healthy mouse strains, with a sample size of five in each group. Bone metastasis was generated through intra-cardiac injection of 1 × 105 tumor cells into 4-week-old female mice, while healthy mice were not subjected to intra-cardiac injection.
3.1 Identification of differential expressed genes (DEGs)
The GEO2R (http://www.ncbi.nlm.nih.gov/geo/geo2r/) web tool was used to compare mRNA expression between breast cancer metastasis and normal tissue samples in mice. The Benjamini and Hochberg false discovery rate (FDR) method was used to filter out false-positive results, and the adjusted p values were calculated. The differentially expressed genes were filtered based on log2 fold change, with a threshold value ≥1 and p < 0.05. To determine the difference among samples and graphically depict the data, we used a built-in tool of GEO2R Uniform Manifold Approximation and Projection (UMAP). A volcano plot showing differentially expressed genes was constructed using the R Language ggplot package.
The receiver operating characteristics (ROC) curve was plotted to determine the specificity and sensitivity of the identified DEGs towards controls and tumor samples using Stata v17.0. The statistical significance level was established as p value < 0.05.
3.2 Network analysis
The protein network analysis of the differentially expressed genes was performed using the STRING database (http://string-db.org), which provides a physical and functional association of proteins. It also provides information about how genes are enriched via various pathways. The functional and pathway enrichment analyses were performed with the cut-off criterion p-value < 0.05. Protein-protein interaction visualization was done through the STRING database.
3.3 Identification of transcription factors and miRNAs binding to DEGs
The Enrichr webtool  was exploited to extract miRNA targeting the identified genes. Significantly (p < 0.05) enriched miRNAs were extracted. The information on protein-protein interactions (PPI) of TFs was also fetched from the Enrichr webtool.
3.4 Molecular docking
3.4.1 Protein preparation
The 3D structure of the targets FABP4 (PDB ID: 3P6D) and IRF4 (PDB ID: 7JM4) were extracted from the Protein Databank. The protein structure of ADGRG7 was extracted from the AlphaFold Protein Structure Database (https://alphafold.ebi.ac.uk/entry/Q96K78). Local minimization of the structure was done by the GROMOS96 (43B1 parameter set) and the Swiss-pdbViewer used for implementation . The CASTp (Computed Atlas of Surface Topography of proteins) web tool was used to extract ligand binding site information .
3.4.2 Preparation of ligand molecules
The three-dimensional structure of the drugs, Actinomycin D (PubChem ID: 31703) and Adriamycin (PubChem ID: 457193), were extracted from the PubChem database . The ligand structures were converted to pdbqt format by OpenBabel software .
3.4.3 Binding in silico
The protein preparation in pdbqt-format was executed using AutodockTools 1.5.4 suite . The molecular docking analysis was performed to develop an improved modeled structure by Autodock Vina Software . After docking analysis, the obtained structures were detected by the Protein-Ligand Interaction Profiler (PLIP) web server (Technical University of Dresden) and tabularized for further analysis .
Figure 1 presents an overview of methods used in present differential expression analysis of macrophages of healthy bone & breast cancer bone metastasis.
4.1 Sample relatedness
The sample and group relationships were identified using the Uniform Manifold Approximation and Projection (UMAP) dimension reduction technique; this provided clustering of the tumor and normal tissues into their respective groups. By color-coding of the sample group on the UMAP, we observed a clear difference between the cancer metastasis group and that of the controls, as shown in Figure 2A, where green depicts the breast cancer bone metastasis samples, and healthy samples are shown in blue-grey.
4.2 Differentially expressed genes
A total of 61 genes were found to be significantly differentially expressed in breast cancer bone metastasis. This included 27 down-regulated genes shown in blue, and 34 up-regulated genes depicted in red (Figure 2B, Supplementary Table S1). Two genes found to be up-regulated by greater than a factor of 3 were Saa3 (Serum amyloid A-3 protein) and Lipg (Supplementary Table S1). They were found to be directly correlated with breast cancer. A new gene, LIPG, was recently found to express and play a role in breast cancer proliferation, tumorigenicity, and metastasis . An acute-phase protein produced by hepatocytes and adipose tissues named Serum amyloid A (SAA) binds to pattern recognition receptors (PRRs), and has a potential role in tumor promotion .
4.3 Functional enrichment analysis
Our results demonstrate that a total of 122 and 105 GO-terms were found to be significantly (FDR < 0.05) enriched for up-regulated genes and down-regulated genes, respectively (Supplementary Tables S2, S3). The top 20 biological processes highly enriched differentially expressed genes were found to be associated with immunological activation and lipid metabolism (Figure 3). The differentially expressed genes were found to be significantly associated with receptor activity and/or binding functions. The differentially expressed genes were major components of the cell membrane or extracellular membrane. Out of 34 up-regulated genes, only 19 genes were found to be associated with the top 20 enriched biological processes that were related to immunological responses. However, 21 down-regulated genes were enriched in the top 20 biological processes associated with lipid metabolism and immunological responses (Supplementary Table S2, S3).
4.4 TFs and miRNAs binding to DEGs
The Enrichr identified 28 miRNAs (Supplementary Table S4) which are targeting DEGs. The miRNA-mRNA interaction map, made by using miRNet v2.0 showed seven of these DEGs having strong interactions with miRNAs (Figure 4). Genes IRF4 and VCAN showed the highest degree of interactions while MRC1 showed the least level of interaction.
Seven significant TFs (p < 0.05) were identified by Enrichr (Figure 5A, Supplementary Table S5). The interactions of these TFs with other proteins/TFs in Figure 5B clearly show strong interaction. The interaction between TFs showed PRDM1 connected with various other TFs which depicted its central role in pathogenesis (Figure 5B).
4.5 ROC analysis
In the Bcl3 gene, the fitted ROC curve is estimated with the assumption of binomial distribution (Figure 6). The parametric estimate of the area under the fitted ROC curve was 0.92 and its 95% confidence interval are 0.73972 and 0.99867. Only the Bcl3 gene showed significant relevance with sensitivity and specificity with the disease as compared to other genes (Supplementary Figure S1A–H).
4.6 Interaction of DEGs and most common drugs used in treatment
The binding site for the target proteins ADGRG7, FABP4 and IRF4 were predicted to be located around ILE (Chain A; Sequence ID: 34), PHE (Chain A; Sequence ID: 16) and GLY (Chain G; Sequence ID: 22), respectively (Figure 7 A–C, Supplementary Table S7–S9). The molecular docking interaction analysis of Actinomycin and Adriamycin drugs, with all the protein targets showed high binding energy (Table 1).
|Protein target||Binding site||Free binding energy (kcal/mol)|
|Chain||Seq ID||Amino acid||Actinomycin||Adriamycin|
The free binding energies of the molecules were found to be ranged from −7.6 to −9.4 kcal/mol. The protein-ligand complex of ADGRG7 with both drugs was observed with the highest binding energy (ADGRG7-Actinomycin complex ∆G = −9.4 kcal/mol; ADGRG7-Adriamycin complex ∆G = −8.1 kcal/mol). The free binding energy of ADGRG7-Actinomycin complex was highest (−)9.4 kcal/mol and the IRF4-Adriamycin complex showed lowest binding energy of (−)7.6 kcal/mol.
The most common site for breast cancer metastases, bone, is involved in about 70% of all metastatic patients [23, 24]. Among breast cancer patients, approximately 14% of patients develop bone metastasis at 15 years post-follow-up . Tumor cells regulate several factors in the bone microenvironment for their maintenance and growth. By releasing cytokines, chemokines, and growth factors, the bone microenvironment inhibits colonization of cancer cells in healthy bones, or supports colonization in cancerous conditions [26, 27]. Production of interferon-γ (IFN-γ) by activated CD4 + T cells inhibits osteoclasts’ activity, thereby protecting bone . Whereas after tumor cell invasion, osteoclastogenesis is promoted by the release of osteoprotegerin (OPG) and cytokines (IL6, IL15 etc.), leading to bone destruction . Thus, an altered balance within the immune system between pro-tumorigenic and anti-tumorigenic molecules decides the fate of tumor cells in bone.
In addition, immune cell plasticity has extensive implications in the pathogenesis and resolution of metabolic disorders: cancers, autoimmune diseases, and chronic inflammatory disorders. In metabolic disorders such as obesity, immune cells interact with various classes of lipids, which can control the plasticity of macrophages and T-lymphocytes. Alterations in lipid metabolism are directly associated with immune cell activation and are also involved in mechanisms associated with several human diseases such as cancer . The proliferation of tumor cells and metastases requires a large amount of energy which is obtained by alterations in lipid metabolism . Several clinical studies have demonstrated high levels of lipids (triglycerides, high density- and low density lipoproteins) in blood plasma of breast cancer patients . Moreover, accumulation of these molecules was correlated with a high propensity of metastases in breast cancer patients. Elevated free fatty acid levels also inhibit fibrin degradation, facilitating breast cancer invasion and metastasis . Thus, a dysregulated immune system and lipid metabolism promote metastases in breast cancer.
This study demonstrates that the up-regulated genes in breast cancer metastases are found to be associated with immune responses. On the other hand, down-regulated genes were involved with the immune response as well as lipid metabolism biological processes (Figure 3).
Four-fold down-regulation of the platelet glycoprotein Cd36 was observed in mouse macrophages of breast cancer bone metastases samples (Table S1). The Cd36 down-regulation was also observed in primary tumor epithelium, and its possible association with breast cancer metastases was reported [34, 35]. Peroxisome proliferator-activated receptor-gamma (PPAR-γ) is a nuclear hormone receptor superfamily transcription factor involved in metabolic functions as well as a suppressor of breast cancer tumors  and was estimated to be down-regulated two-fold in tumors. Similarly, other downregulated genes (Fabp4, Mrc1, Lpl, Cd209d, and Cd209a) were also found to be involved in breast cancer and may be associated with bone metastases. However, further investigation is required to confirm their association with bone metastases. Lipoprotein lipase (Lpl) was observed to be depleted in the disease condition (Table S1). Lpl functions as a triglyceride hydrolase and receptor-mediated factor for lipoprotein uptake . Loss of Lpl expression was reported to be directly associated with lipid metabolism and to cause hyperlipidemia [38, 39]. A previous study suggests that down-regulation of Lpl may be the result of epigenetic alterations, such as CpG island hypermethylation and/or histone modification . Altered genomic DNA is also reported to contribute to the loss of Lpl. The cancer susceptibility gene deleted in breast cancer (Dcb2), known as Rho-related BTB domain containing 2 (Rohbtb2), mapped closed to the Lpl gene which may also be affected by Lpl deletion and could therefore exert a combined impact on promoting carcinogenesis [40, 41]. Lpl is found to suppress TNFa and IFNg associated inflammation activating genes through inactivation of transcription factor NF-kB [40, 42]. Therefore, loss of Lpl activity may promote carcinogenesis.
Several significantly up-regulated genes were identified in the macrophages in the cancer phenotype. One of the up-regulated genes, Bcl3 was found to be approximately two and a half times higher than the controls. It is a transcription co-activator proto-oncogene and a candidate for therapeutic intervention of disease progression. Bcl3 is aberrantly expressed in tumors, including breast cancer. Although the role of Bcl3 in tumor pathology is poorly understood, it mediates transcription suppression of NF-kB signaling and affects metastasis-associated genes. Bcl3 deficiency was found with only minor immunologic defects. Therefore, it may also be considered a plausible drug target . Interleukin-1 receptor type 2 (IL1R2), was discovered to be a negative immune regulator, and is three-fold up-regulated in pathologic cases (Table S1). IL1R2 binds and increases the activity of the ubiquitin-specific protease 15 (USP15) in breast cancer cells. IL1R2 promotes the self-renewal of breast tumor-initiating cells, as well as cancer proliferation and invasion . However, USP15 is a deubiquitinase and was found to be involved in several cellular signaling pathways such as COP9-signalosome, NFκB, and p53 signaling pathways . The in vitro and in vivo study suggested that overexpression of IL1R2 leads to down-regulation of USP15, and helps in controlling breast cancer malignancy. Therefore, IL1R2 was reported to be a potential therapeutic target for breast cancer treatment . Additionally, the cytokines and chemokines (Cxcl10, Cxcl9, and Cxcr3) were found to be up-regulated (Table S1) in the phenotype. These factors are suggested to play a role in driving cancer cell proliferation in the bone microenvironment .
Further, the extended analysis using Enrichr showed several crucial miRNAs like miR-138-5p, miR-26a-5p, miR-574-5p, hsa-miR-331-5p (Supplementary Table S4) which are targeting to DEGs. The miR-138-5p and miR-331 are associated with cell migration and invasion ability of breast cancer cells [47–49]. The miR-497 suppresses proliferation and induces apoptosis in breast cancer cells by targeting Bcl-w gene . The miR-26a-5p is a well known tumor oncogene for osteosarcoma  and is also known to inhibit breast cancer cell growth . The miR-26a-5p was found to be remarkably upregulated in osteosarcoma patients and significantly correlated with poor prognosis . The miR-574-5p was found to be highly related to development and metastasis of breast cancer . It was reported actively involved in the Wnt/β-catenin signaling pathway and plays crucial role in bone metastasis in non-small cell lung cancer (NSCLC) patients . These miRNAs target identified DEGs which is evident from Figure 4 and Supplementary Table S4 and their interaction have been proven experimentally in literature. The miR-497 suppresses proliferation and induces apoptosis in breast cancer cells by targeting Bcl-w gene .
The Enrichr also showed several significant TFs (p < 0.05) which are interacting with identified DEGs (Supplementary Table S5, Figure 5A). The IRF8 (Interferon regulatory factor 8) and BATF (Basic Leucine Zipper ATF-Like Transcription Factor) are very crucial in developing the anti-tumour response in tumour surveillance. IRF and BATF negative mice had a fast rate of tumour development [56, 57]. Notably, these TFs and other TFs like STAT6 and CCDN1 are directly involved in developing breast cancer and its metastasis [58–60]. Deregulated levels of these TFs are correlated with unfavorable relapse-free survival of patients. The ROC analysis showed that Bcl3 gene possessed highest specificity and sensitivity to distinguish cancer and control samples while other identified genes failed to correlate with that (Figure 6, Supplementary Figure S1A–H, supplementary Table S6).
Selected genes were analysed for their binding to most common anti-tumour drugs (Actinomycin-D and Adrimycin) by molecular docking (Figure 7, Supplementary Table S7–S9). The Actinomycin-D (Act-D) is a well-known potent anticancer drug produced by Streptomyces bacteria. The high toxicity caused by Act-D is attributed to its ability to inhibit transcription of several important gene such as c-myc, c-met, myotonic Dystrophy type 1 etc. Importantly, it has been approved by the FDA for multiple tumors, Wilms’ tumor and gestational choriocarcinoma and in combination with other drugs to treat high risk tumor in chemotherapy regime [61–63]. The chemical structure of Act-D comprises planar phenoxazone ring and two cyclic pentapeptide lactones, a very heavy molecule . The Adriamycin (synonym doxorubicin) is a glycoside antibiotic whose structure and stereochemistry are represented in Figure 6 (formula I). It consists of the tetracyclic quinoid aglycone adriamycinone (l4-hydroxydaunomycinone) linked to the aminosugar daunosamine [64, 65]. Both drugs were found to bind selected genes (ADGRG7, FABP4, IRF4) efficiently (free energy −7.6–9.4 kcal/mol; Table 1).
The study unveiled various deregulated genes demonstrating a strong role in bone metastasis of breast cancer macrophages. Distinct and altered signaling pathways were identified and it was determined that their key genes are likely involved in promoting carcinogenesis. Deregulated genes in lipid metabolism are directly involved in immunological responses, which in turn promote cancer and its spread to bone. The molecular docking study revealed that the identified deregulated genes (ADGRG-7 and IRF4) have vital anticancer drugs (Actinomycin-D and Adriamycin) targets. ROC analysis showed BCl3 gene was most specific with breast cancer-associated bone metastasis. The extended analysis by Enrichr identified miRNAs and TFs which are directly involved in the crucial pathological mechanism. However, their exact role in the pathophysiology of bone metastasis needs to be investigated within in vitro conditions.
In breast cancer bone metastasis, most immunological molecules such as chemokines, cytokines, and lipid metabolism molecules were found to be altered. These identified altered pathways promote bone metastasis outgrowth and prolonged survival of tumor cells. Some of the up-regulated genes such as Bcl3, Cxcl10, and Cxcr3; miRNAs (miR-497, miR-574, miR-138) and TFs (IRF8, STAT6, CCDN1) associated with metastasis may also be plausible targets for future therapeutics. However, in vitro and in vivo studies are required to confirm the role of these identified genes and pathways in the pathogenesis.
Author contribution: All authors wrote the paper and critically commented to the manuscript. All authors read and approved the final manuscript.
Research funding: None declared.
Conflict of interest statement: There are no conflicts of interest.
1. Pan, Y, Lin, Y, Mi, C. Clinicopathological characteristics and prognostic risk factors of breast cancer patients with bone metastasis. Ann Transl Med 2021;9:1340. https://doi.org/10.21037/atm-21-4052.Search in Google Scholar PubMed PubMed Central
3. Caswell-Jin, JL, Plevritis, SK, Tian, L, Cadham, CJ, Xu, C, Stout, NK, et al.. Change in survival in metastatic breast cancer with treatment advances: meta-analysis and systematic review. JNCI Cancer Spectr 2018;2:pky062. https://doi.org/10.1093/jncics/pky062.Search in Google Scholar PubMed PubMed Central
4. Pulido, C, Vendrell, I, Ferreira, AR, Casimiro, S, Mansinho, A, Alho, I, et al.. Bone metastasis risk factors in breast cancer. Ecancermedicalscience 2017;11:715. https://doi.org/10.3332/ecancer.2017.715.Search in Google Scholar PubMed PubMed Central
5. Macedo, F, Ladeira, K, Pinho, F, Saraiva, N, Bonito, N, Pinto, L, et al.. Bone metastases: an overview. Onco Rev 2017;11:321. https://doi.org/10.4081/oncol.2017.321.Search in Google Scholar PubMed PubMed Central
7. Patel, JP, Deshmukh, S, Zhao, C, Wamuo, O, Hsu, SL, Schoch, AB, et al.. An analysis of the role of nonreactive plasticizers in the crosslinking reactions of a rigid resin. J Polym Sci B Polym Phys 2017;55:206–13. https://doi.org/10.1002/polb.24261.Search in Google Scholar
8. Patel, JP, Xiang, ZG, Hsu, SL, Schoch, AB, Carleen, AA, Matsumoto, D. Path to achieving molecular dispersion in a dense reactive mixture. J Polym Sci B Polym Phys 2017;53:1519–26. https://onlinelibrary.wiley.com/doi/abs/10.1002/polb.23789.10.1002/polb.23789Search in Google Scholar
9. Xu, D, Wang, H-W, Patel, J, Brun, XF, Hirota, K, Capsuto, E, et al.. A novel design of temporary Bond debond adhesive technology for wafer-level assembly. In: 2020 IEEE 70th Electronic Components and Technology Conference (ECTC); 2020. pp. 68–74.10.1109/ECTC32862.2020.00024Search in Google Scholar
10. Sharma, A, Jain, N, Sareen, R. Nanocarriers for diagnosis and targeting of breast cancer. BioMed Res Int 2013;2013:960821. https://doi.org/10.1155/2013/960821.Search in Google Scholar PubMed PubMed Central
11. Salerno, M, Cenni, E, Fotia, C, Avnet, S, Granchi, D, Castelli, F, et al.. Bone-targeted doxorubicin-loaded nanoparticles as a tool for the treatment of skeletal metastases. Curr Cancer Drug Targets 2010;10:649–59. https://doi.org/10.2174/156800910793605767.Search in Google Scholar PubMed
12. Lin, S, Zhang, C, Liu, F, Ma, J, Jia, F, Han, Z, et al.. Actinomycin V inhibits migration and invasion via suppressing snail/slug-mediated epithelial-mesenchymal transition progression in human breast cancer MDA-MB-231 cells in vitro. Mar Drugs 2019:305. https://doi.org/10.3390/md17050305.Search in Google Scholar PubMed PubMed Central
13. Chen, EY, Tan, CM, Kou, Y, Duan, Q, Wang, Z, Meirelles, GV, Clark, NR, Ma’ayan, A. Enrichr: interactive and collaborative HTML5 gene list enrichment analysis tool. BMC Bioinf 2013;14:128. https://doi.org/10.1186/1471-2105-14-128.Search in Google Scholar PubMed PubMed Central
14. Johansson, MU, Zoete, V, Michielin, O, Guex, N. Defining and searching for structural motifs using DeepView/Swiss-PdbViewer. BMC Bioinf 2012;13:173. https://doi.org/10.1186/1471-2105-13-173.Search in Google Scholar PubMed PubMed Central
15. Tian, W, Chen, C, Lei, X, Zhao, J, Liang, J. CASTp 3.0: computed atlas of surface topography of proteins. Nucleic Acids Res 2018;46:W363–7. https://doi.org/10.1093/nar/gky473.Search in Google Scholar PubMed PubMed Central
16. Kim, S, Chen, J, Cheng, T, Gindulyte, A, He, J, He, S, et al.. PubChem in 2021: new data content and improved web interfaces. Nucleic Acids Res 2021;49:D1388–95. https://doi.org/10.1093/nar/gkaa971.Search in Google Scholar PubMed PubMed Central
17. O’Boyle, NM, Banck, M, James, CA, Morley, C, Vandermeersch, T, Hutchison, GR. Open Babel: an open chemical toolbox. J Cheminf 2011;3:33. https://doi.org/10.1186/1758-2946-3-33.Search in Google Scholar PubMed PubMed Central
18. Morris, GM, Huey, R, Lindstrom, W, Sanner, MF, Belew, RK, Goodsell, DS, et al.. AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility. J Comput Chem 2009;30:2785–91. https://doi.org/10.1002/jcc.21256.Search in Google Scholar PubMed PubMed Central
19. Trott, O, Olson, AJ. AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J Comput Chem 2010;31:455–61. https://doi.org/10.1002/jcc.21334.Search in Google Scholar PubMed PubMed Central
20. Salentin, S, Schreiber, S, Haupt, VJ, Adasme, MF, Schroeder, M. PLIP: fully automated protein-ligand interaction profiler. Nucleic Acids Res 2015;43:W443–447. https://doi.org/10.1093/nar/gkv315.Search in Google Scholar PubMed PubMed Central
21. Cadenas, C, Vosbeck, S, Edlund, K, Grgas, K, Madjar, K, Hellwig, B, et al.. LIPG-promoted lipid storage mediates adaptation to oxidative stress in breast cancer. Int J Cancer 2019;145:901–15. https://doi.org/10.1002/ijc.32138.Search in Google Scholar PubMed PubMed Central
22. Fourie, C, Shridas, P, Davis, T, de Villiers, WJS, Engelbrecht, A-M. Serum amyloid A and inflammasome activation: a link to breast cancer progression? Cytokine Growth Factor Rev 2021;59:62–70. https://doi.org/10.1016/j.cytogfr.2020.10.006.Search in Google Scholar PubMed
23. Manders, K, van de Poll-Franse, LV, Creemers, G-J, Vreugdenhil, G, van der Sangen, MJC, Nieuwenhuijzen, GAP, et al.. Clinical management of women with metastatic breast cancer: a descriptive study according to age group. BMC Cancer 2006;6:179. https://doi.org/10.1186/1471-2407-6-179.Search in Google Scholar PubMed PubMed Central
24. Kennecke, H, Yerushalmi, R, Woods, R, Cheang, MCU, Voduc, D, Speers, CH, et al.. Metastatic behavior of breast cancer subtypes. J Clin Oncol 2010;28:3271–7. https://doi.org/10.1200/JCO.2009.25.9820.Search in Google Scholar PubMed
25. Liede, A, Jerzak, KJ, Hernandez, RK, Wade, SW, Sun, P, Narod, SA. The incidence of bone metastasis after early-stage breast cancer in Canada. Breast Cancer Res Treat 2016;156:587–95. https://doi.org/10.1007/s10549-016-3782-3.Search in Google Scholar PubMed
26. Peinado, H, Zhang, H, Matei, IR, Costa-Silva, B, Hoshino, A, Rodrigues, G, et al.. Pre-metastatic niches: organ-specific homes for metastases. Nat Rev Cancer 2017;17:302–17. https://doi.org/10.1038/nrc.2017.6.Search in Google Scholar PubMed
28. Xu, Z, Hurchla, MA, Deng, H, Uluçkan, O, Bu, F, Berdy, A, et al.. Interferon-gamma targets cancer cells and osteoclasts to prevent tumor-associated bone loss and bone metastases. J Biol Chem 2009;284:4658–66. https://doi.org/10.1074/jbc.M804812200.Search in Google Scholar PubMed PubMed Central
29. Sawant, A, Hensel, JA, Chanda, D, Harris, BA, Siegal, GP, Maheshwari, A, et al.. Depletion of plasmacytoid dendritic cells inhibits tumor growth and prevents bone metastasis of breast cancer cells. J Immunol (Baltimore, Md: 1950) 2012;189:4258–65. https://doi.org/10.4049/jimmunol.1101855.Search in Google Scholar PubMed PubMed Central
30. Hubler, MJ, Kennedy, AJ. Role of lipids in the metabolism and activation of immune cells. J Nutr Biochem 2016;34:1–7. https://doi.org/10.1016/j.jnutbio.2015.11.002.Search in Google Scholar PubMed PubMed Central
31. Zhu, Y, Aupperlee, MD, Zhao, Y, Tan, YS, Kirk, EL, Sun, X, et al.. Pubertal and adult windows of susceptibility to a high animal fat diet in Trp53-null mammary tumorigenesis. Oncotarget 2016;7:83409–23. https://doi.org/10.18632/oncotarget.13112.Search in Google Scholar
32. Wei, LJ, Zhang, C, Zhang, H, Wei, X, Li, SX, Liu, JT, et al.. A case-control study on the association between serum lipid level and the risk of breast cancer. Zhonghua Yu Fang Yi Xue Za Zhi [Chinese Journal of Preventive Medicine] 2016;50:1091–5. https://doi.org/10.3760/cma.j.issn.0253-9624.2016.12.013.Search in Google Scholar
33. Byon, CH, Hardy, RW, Ren, C, Ponnazhagan, S, Welch, DR, McDonald, JM, et al.. Free fatty acids enhance breast cancer cell migration through plasminogen activator inhibitor-1 and SMAD4. Lab Invest 2009;89:1221–8. https://doi.org/10.1038/labinvest.2009.97.Search in Google Scholar
34. Johnstone, CN, Smith, YE, Cao, Y, Burrows, AD, Cross, RSN, Ling, X, et al.. Functional and molecular characterisation of EO771.LMB tumours, a new C57BL/6-mouse-derived model of spontaneously metastatic mammary cancer. Dis Models Mech 2015;8:237–51. https://doi.org/10.1242/dmm.017830.Search in Google Scholar
35. Enciu, A-M, Radu, E, Popescu, ID, Hinescu, ME, Ceafalan, LC. Targeting CD36 as biomarker for metastasis prognostic: how far from translation into clinical practice? BioMed Res Int 2018;2018:7801202. https://doi.org/10.1155/2018/7801202.Search in Google Scholar
36. Rovito, D, Gionfriddo, G, Barone, I, Giordano, C, Grande, F, De Amicis, F, et al.. Ligand-activated PPARγ downregulates CXCR4 gene expression through a novel identified PPAR response element and inhibits breast cancer progression. Oncotarget 2016;7:65109–24. https://doi.org/10.18632/oncotarget.11371.Search in Google Scholar
37. Miller, AL, Smith, LC. Activation of lipoprotein lipase by apolipoprotein glutamic acid. Formation of a stable surface film. J Biol Chem 1973;248:3359–62.10.1016/S0021-9258(19)44049-0Search in Google Scholar
38. Gehrisch, S. Common mutations of the lipoprotein lipase gene and their clinical significance. Curr Atherosclerosis Rep 1999;1:70–8. https://doi.org/10.1007/s11883-999-0052-4.Search in Google Scholar PubMed
39. Mead, JR, Irvine, SA, Ramji, DP. Lipoprotein lipase: structure, function, regulation, and role in disease. J Mol Med 2002;80:753–69. https://doi.org/10.1007/s00109-002-0384-9.Search in Google Scholar PubMed
40. Takasu, S, Mutoh, M, Takahashi, M, Nakagama, H. Lipoprotein lipase as a candidate target for cancer prevention/therapy. Biochem Res Int 2012;2012:398697. https://doi.org/10.1155/2012/398697.Search in Google Scholar PubMed PubMed Central
41. Knowles, MA, Aveyard, JS, Taylor, CF, Harnden, P, Bass, S. Mutation analysis of the 8p candidate tumour suppressor genes DBC2 (RHOBTB2) and LZTS1 in bladder cancer. Cancer Lett 2005;225:121–30. https://doi.org/10.1016/j.canlet.2004.10.047.Search in Google Scholar PubMed
42. Kota, RS, Ramana, CV, Tenorio, FA, Enelow, RI, Rutledge, JC. Differential effects of lipoprotein lipase on tumor necrosis factor-alpha and interferon-gamma-mediated gene expression in human endothelial cells. J Biol Chem 2005;280:31076–84. https://doi.org/10.1074/jbc.M412189200.Search in Google Scholar PubMed
43. Schwarz, EM, Krimpenfort, P, Berns, A, Verma, IM. Immunological defects in mice with a targeted disruption in Bcl-3. Genes Dev 1997;11:187–97. https://doi.org/10.1101/gad.11.2.187.Search in Google Scholar PubMed
44. Zhang, L, Qiang, J, Yang, X, Wang, D, Rehman, AU, He, X, et al.. IL1R2 blockade suppresses breast tumorigenesis and progression by impairing USP15-dependent BMI1 stability. Adv Sci 2020;7:1901728. https://doi.org/10.1002/advs.201901728.Search in Google Scholar PubMed PubMed Central
45. Chou, C-K, Chang, Y-T, Korinek, M, Chen, Y-T, Yang, Y-T, Leu, S, et al.. The regulations of deubiquitinase USP15 and its pathophysiological mechanisms in diseases. Int J Mol Sci 2017;18:E483. https://doi.org/10.3390/ijms18030483.Search in Google Scholar PubMed PubMed Central
46. Romero-Moreno, R, Curtis, KJ, Coughlin, TR, Miranda-Vergara, MC, Dutta, S, Natarajan, A, et al.. The CXCL5/CXCR2 axis is sufficient to promote breast cancer colonization during bone metastasis. Nat Commun 2019;10:4404. https://doi.org/10.1038/s41467-019-12108-6.Search in Google Scholar PubMed PubMed Central
47. Zhao, C, Ling, X, Li, X, Hou, X, Zhao, D. MicroRNA-138-5p inhibits cell migration, invasion and EMT in breast cancer by directly targeting RHBDD1. Breast Cancer 2019;26:817–25. https://doi.org/10.1007/s12282-019-00989-w.Search in Google Scholar PubMed
48. Karagkouni, D, Paraskevopoulou, MD, Chatzopoulos, S, Vlachos, IS, Tastsoglou, S, Kanellos, I, et al.. DIANA-TarBase v8: a decade-long collection of experimentally supported miRNA-gene interactions. Nucleic Acids Res 2018;46:D239−45. https://doi.org/10.1093/nar/gkx1141.Search in Google Scholar PubMed PubMed Central
49. McAnena, P, Tanriverdi, K, Curran, C, Gilligan, K, Freedman, JE, Brown, JAL, et al.. Circulating microRNAs miR-331 and miR-195 differentiate local luminal a from metastatic breast cancer. BMC Cancer 2019;19:436. https://doi.org/10.1186/s12885-019-5636-y.Search in Google Scholar PubMed PubMed Central
50. Shen, L, Li, J, Xu, L, Ma, J, Li, H, Xiao, X, et al.. MiR-497 induces apoptosis of breast cancer cells by targeting Bcl-w. Exp Ther Med 2012;3:475–80. https://doi.org/10.3892/etm.2011.428.Search in Google Scholar PubMed PubMed Central
51. Yu, T, Chen, D, Zhang, L, Wan, D. MicroRNA-26a-5p promotes proliferation and migration of osteosarcoma cells by targeting HOXA5 in vitro and in vivo. OncoTargets Ther 2019;12:11555–65. https://doi.org/10.2147/OTT.S232100.Search in Google Scholar PubMed PubMed Central
52. Huang, Z-M, Ge, H-F, Yang, C-C, Cai, Y, Chen, Z, Tian, W-Z, et al.. MicroRNA-26a-5p inhibits breast cancer cell growth by suppressing RNF6 expression. Kaohsiung J Med Sci 2019;35:467–73. https://doi.org/10.1002/kjm2.12085.Search in Google Scholar PubMed
53. Xie, X-Y, Chen, X-M, Shi, L, Liu, J-W. Increased expression of microRNA-26a-5p predicted a poor survival outcome in osteosarcoma patients: an observational study. Medicine 2021;100: e24765. https://doi.org/10.1097/MD.0000000000024765.Search in Google Scholar PubMed
54. Wang, P-S, Chou, C-H, Lin, C-H, Yao, Y-C, Cheng, H-C, Li, H-Y, et al.. A novel long non-coding RNA linc-ZNF469-3 promotes lung metastasis through miR-574-5p-ZEB1 axis in triple negative breast cancer. Oncogene 2018;37:4662–78. https://doi.org/10.1038/s41388-018-0293-1.Search in Google Scholar PubMed
55. Yang, X-R, Pi, C, Yu, R, Fan, X-J, Peng, X-X, Zhang, X-C, et al.. Correlation of exosomal microRNA clusters with bone metastasis in non-small cell lung cancer. Clin Exp Metastasis 2021;38:109–17. https://doi.org/10.1007/s10585-020-10062-y.Search in Google Scholar PubMed PubMed Central
56. Hildner, K, Edelson, BT, Purtha, WE, Diamond, M, Matsushita, H, Kohyama, M, et al.. Batf3 deficiency reveals a critical role for CD8alpha + dendritic cells in cytotoxic T cell immunity. Science (New York, N.Y.) 2008;322:1097–100. https://doi.org/10.1126/science.1164206.Search in Google Scholar PubMed PubMed Central
57. Meyer, MA, Baer, JM, Knolhoff, BL, Nywening, TM, Panni, RZ, Su, X, et al.. Breast and pancreatic cancer interrupt IRF8-dependent dendritic cell development to overcome immune surveillance. Nat Commun 2018;9:1250. https://doi.org/10.1038/s41467-018-03600-6.Search in Google Scholar PubMed PubMed Central
58. Cerami, E, Gao, J, Dogrusoz, U, Gross, BE, Sumer, SO, Aksoy, BA, et al.. The cBio cancer genomics portal: an open platform for exploring multidimensional cancer genomics data. Cancer Discov 2012;2:401–4. https://doi.org/10.1158/2159-8290.CD-12-0095.Search in Google Scholar PubMed PubMed Central
59. DiScala, M, Najor, MS, Yung, T, Morgan, D, Abukhdeir, AM, Cobleigh, MA. Loss of STAT6 leads to anchorage-independent growth and trastuzumab resistance in HER2+ breast cancer cells. PLoS One 2020;15: e0234146. https://doi.org/10.1371/journal.pone.0234146.Search in Google Scholar PubMed PubMed Central
61. Lohani, N, Singh, HN, Moganty, RR. Structural aspects of the interaction of anticancer drug Actinomycin-D to the GC rich region of hmgb1 gene. Int J Biol Macromol 2016;87:433–42. https://doi.org/10.1016/j.ijbiomac.2016.02.060.Search in Google Scholar PubMed
62. Lohani, N, Singh, HN, Rajeswari, MR. Assessment of binding properties of Actinomycin-D to 21nt DNA segment of hmgb1 gene promoter using spectroscopic and calorimetric techniques. J Biomol Struct Dynam 2018;36:504–11. https://doi.org/10.1080/07391102.2016.1278037.Search in Google Scholar PubMed
63. Lu, D-F, Wang, Y-S, Li, C, Wei, G-J, Chen, R, Dong, D-M, et al.. Actinomycin D inhibits cell proliferations and promotes apoptosis in osteosarcoma cells. Int J Clin Exp Med 2015;8:1904–11.Search in Google Scholar
64. Yun, C, Lee, JH, Park, H, Jin, YM, Park, S, Park, K, et al.. Chemotherapeutic drug, adriamycin, restores the function of p53 protein in hepatitis B virus X (HBx) protein-expressing liver cells. Oncogene 2000;19:5163–72. https://doi.org/10.1038/sj.onc.1203896.Search in Google Scholar PubMed
65. Lohani, N, Narayan Singh, H, Agarwal, S, Mehrotra, R, Rajeswari, MR. Interaction of adriamycin with a regulatory element of hmgb1: spectroscopic and calorimetric approach. J Biomol Struct Dynam 2015;33:1612–23. https://doi.org/10.1080/07391102.2014.967301.Search in Google Scholar PubMed
The online version of this article offers supplementary material (https://doi.org/10.1515/jib-2021-0041).
© 2022 Yashbir Singh et al., published by De Gruyter, Berlin/Boston
This work is licensed under the Creative Commons Attribution 4.0 International License.