4.5 Article

Dual function miR-205 is positively associated with ER and negatively with five-year survival in breast cancer patients

期刊

PATHOLOGY RESEARCH AND PRACTICE
卷 238, 期 -, 页码 -

出版社

ELSEVIER GMBH
DOI: 10.1016/j.prp.2022.154080

关键词

Triple-negative breast cancer; Estrogen receptor-positive breast cancer; MiR-205; Chemotherapy; Hormone therapy; Survival

资金

  1. Ministry of Education, Science and Technological Development of the Republic of Serbia [451-03-9/2021-14/200017]

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This study aimed to investigate the expression of miR-205 in different subtypes of breast cancer and its association with clinical characteristics and prognosis. The results showed that the expression of miR-205 is subtype-specific, with high expression being associated with ER-positive tumors. The expression level of miR-205 may serve as a useful biomarker for predicting TNBC progression.
Background: Precise molecular characterization of breast cancer, especially triple negative (TNBC) as the most lethal subtype, is needed to stratify patients for the individual treatment approach. MicroRNA-205 (miR-205) has tumor-suppressive and oncogenic functions across different cancers. Therefore, miR-205 might have a different role in TNBC and estrogen receptor (ER) positive BC. Our aim was to investigate how miR-205 expression is associated with ER/progesteron receptor status, clinical parameters, pathohistological characteristics of BC, and survival of patients Methods: We determined miR-205 relative expressions in 73 primary breast tumors (50 TNBC and 23 ER+) by quantitative Real-time polymerase chain reaction (qPCR) and compared it to clinicopathological characteristics and outcome. Results: The highest levels of miR-205 were in the ER+ /PR+ group, and the lowest in the TNBC group (p = 0.009). Significantly higher levels of miR-205 were also observed in the ER+ compared with the ER-negative group, regardless of the PR status (p = 0.002). Low miR-205 expression level was associated with prognostic stage III in TNBC samples (p = 0.049). Patients who received adjuvant chemotherapy had significantly lower levels of miR-205 (p = 0.016). Patients who received hormone therapy had significantly higher levels of miR-205 (p = 0.007). The low-miR-205 patients had significantly higher 5-year survival rates (p = 0.041). Conclusion: The expression of miR-205 in BC is subtype-specific and high expression is associated with the ER+ tumors. The miR-205 expression might be a useful marker of TNBC progression. High miR-205 expression had a detrimental effect on BC patient outcome. Our results indicate that miR-205 might be utilized in clinical practice as a biomarker and an adjunct parameter for the selection of the most effective therapeutic modality.

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