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pmid:35685372

Deregulated molecules and pathways in the predisposition and dissemination of breast cancer cells to bone.

Laijian Sui · Andrew Sanders · Wen G Jiang · Lin Ye

Computational and structural biotechnology journal · 2022 doi:10.1016/j.csbj.2022.05.051

Paper

complete

Experiment

partial

Data

partial

Analysis

partial

Execution

absent

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Deregulated molecules and pathways in the predisposition and dissemination of breast cancer cells to bone.
doi
10.1016/j.csbj.2022.05.051
pmid
35685372
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Laijian Sui
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Andrew Sanders
[2]
Wen G Jiang
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Lin Ye
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Computational and structural biotechnology journal
year
2022
abstract
Background: Bone metastasis is the most common metastatic destination in advanced breast cancer, presenting a poor prognosis and clinical challenges in management. To date, the mechanism of bone metastasis in breast cancer remains largely unclear. Methods: Differentially expressed genes in primary tumours that developed bone metastases were systematically analysed using both TCGA-BRCA and E-MTAB-4003 databases. Adaptive phenotype in the subsequent bone lesions was analysed in the GSE46161 database. A series of biomarkers including homing, immune escape, angiogenesis, and factors involved in both osteoblastogenesis and osteoclastogenesis were included to dissect the molecular events underlying bone metastasis in breast cancer. Results: Upregulated expressions of GDF11 expression is positively correlated with colonization, osteoblastogenesis and osteoclastogenesis, whilst CD151 is positively associated with angiogenesis and immune escape. PAFAH1B2 expression is inversely correlated with the angiogenic process. Reduced YTHDF2 may facilitate cancer cell homing, osteoclastogenesis and immune escape in breast cancer. DPP9, FAS, ZNF519, RPP14 and FAU were evaluated for their potential involvement in for the homing to bone, escaping from immune surveillance, angiogenesis, osteoblastic activity and osteoclastic activity in the multi-step process of bone metastasis. Conclusion: GDF11, CD151, PAFAH1B2 and YTHDF2 may play a pivotal role in the predisposition of metastasis to the bone from breast cancer, whilst DPP9, FAS, ZNF519, RPP14 and FAU may be actively involved in the adaptative colonisation of metastatic breast cancer cells in bone.
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Normally distributed data was analysed by student T-test, whilst non-normally distributed data was assessed using Mann-Whitney tests. Bone metastasis free survival was assessed using Kaplan-Meier tests in TCGA-BRCA database. Correlation with markers of homing, osteoclastogenesis, osteoblastogenesis, immune-escape and neo-angiogenesis was evaluated using Spearman test.
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Normally distributed data was analysed by student T-test, whilst non-normally distributed data was assessed using Mann-Whitney tests. Bone metastasis free survival was assessed using Kaplan-Meier tests in TCGA-BRCA database. Correlation with markers of homing, osteoclastogenesis, osteoblastogenesis, immune-escape and neo-angiogenesis was evaluated using Spearman test.
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RNA sequencing data of a cohort of breast cancer tumours (n = 1093) from The Cancer Gene Atlas (TCGA) was analysed as a cohort for discovery in the present study to evaluate differentially expressed genes (DEGs) in breast cancer with distant metastasis (n = 123), especially with bone metastasis (n = 58).
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RNA sequencing data of a cohort of breast cancer tumours (n = 1093) from The Cancer Gene Atlas (TCGA) was analysed as a cohort for discovery in the present study to evaluate differentially expressed genes (DEGs) in breast cancer with distant metastasis (n = 123), especially with bone metastasis (n = 58).
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GDF11, CD151, PAFAH1B2 and YTHDF2 may play a pivotal role in the predisposition of metastasis to the bone from breast cancer, whilst DPP9, FAS, ZNF519, RPP14 and FAU may be actively involved in the adaptative colonisation of metastatic breast cancer cells in bone.
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GDF11, CD151, PAFAH1B2 and YTHDF2 may play a pivotal role in the predisposition of metastasis to the bone from breast cancer, whilst DPP9, FAS, ZNF519, RPP14 and FAU may be actively involved in the adaptative colonisation of metastatic breast cancer cells in bone.
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GDF11, CD151, PAFAH1B2 and YTHDF2 may play a pivotal role in the predisposition of metastasis to the bone from breast cancer, whilst DPP9, FAS, ZNF519, RPP14 and FAU may be actively involved in the adaptative colonisation of metastatic breast cancer cells in bone.
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Normally distributed data was analysed by student T-test, whilst non-normally distributed data was assessed using Mann-Whitney tests. Bone metastasis free survival was assessed using Kaplan-Meier tests in TCGA-BRCA database. Correlation with markers of homing, osteoclastogenesis, osteoblastogenesis, immune-escape and neo-angiogenesis was evaluated using Spearman test.
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RNA sequencing data of a cohort of breast cancer tumours (n = 1093) from The Cancer Gene Atlas (TCGA) was analysed as a cohort for discovery in the present study to evaluate differentially expressed genes (DEGs) in breast cancer with distant metastasis (n = 123), especially with bone metastasis (n = 58).
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Normally distributed data was analysed by student T-test, whilst non-normally distributed data was assessed using Mann-Whitney tests. Bone metastasis free survival was assessed using Kaplan-Meier tests in TCGA-BRCA database. Correlation with markers of homing, osteoclastogenesis, osteoblastogenesis, immune-escape and neo-angiogenesis was evaluated using Spearman test.
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To date, the mechanism of bone metastasis in breast cancer remains largely unclear.\nMethods: Differentially expressed genes in primary tumours that developed bone metastases were systematically analysed using both TCGA-BRCA and E-MTAB-4003 databases. Adaptive phenotype in the subsequent bone lesions was analysed in the GSE46161 database. A series of biomarkers including homing, immune escape, angiogenesis, and factors involved in both osteoblastogenesis and osteoclastogenesis were included to dissect the molecular events underlying bone metastasis in breast cancer.\nResults: Upregulated expressions of GDF11 expression is positively correlated with colonization, osteoblastogenesis and osteoclastogenesis, whilst CD151 is positively associated with angiogenesis and immune escape. PAFAH1B2 expression is inversely correlated with the angiogenic process. Reduced YTHDF2 may facilitate cancer cell homing, osteoclastogenesis and immune escape in breast cancer. 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