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The HSP70 gene predicts prognosis and response to chemotherapy in epithelial ovarian cancer
Chemotherapy resistance is an intractable problem in treating patients with epithelial ovarian cancer (EOC). Heat shock proteins (HSPs) act as apoptosis inhibitors and are highly conserved genetically. Most HSPs have strong cytoprotective effects, and their overexpression inhibits apoptosis. This ha...
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Published in: | Annals of translational medicine 2021-05, Vol.9 (9), p.806-806 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that cite this one |
Online Access: | Get full text |
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Summary: | Chemotherapy resistance is an intractable problem in treating patients with epithelial ovarian cancer (EOC). Heat shock proteins (HSPs) act as apoptosis inhibitors and are highly conserved genetically. Most HSPs have strong cytoprotective effects, and their overexpression inhibits apoptosis. This has been demonstrated for
. Heat shock protein 70 (
) expression is abnormally upregulated in malignant cells. Furthermore,
can inhibit cell death and promote chemotherapeutic resistance. In our study, the relationship between the
gene and primary chemotherapy resistance and clinical outcome in patients with EOC was explored.
Quantitative real-time polymerase chain (qRT-PCR) was applied to determine
messenger RNA (mRNA) levels, and immunohistochemistry assay was conducted to determine
protein level.
overexpression was assessed to clarify its role on chemotherapy resistance to cisplatin in SKOV3 cell lines.
RT-qPCR assay indicated a strong relationship between
expression and chemotherapy resistance in patients with EOC. In cultured SKOV3 cells, overexpression of
inhibited cell sensitivity to cisplatin. Kaplan-Meier analysis demonstrated high
expression was associated with poor outcome of EOC patients. In multivariate models, high
expression independently predicted this poor outcome.
predicts the prognosis and response to chemotherapy in EOC patients. |
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ISSN: | 2305-5839 2305-5839 |
DOI: | 10.21037/atm-21-2087 |