ArticleInternational journal of clinical and experimental pathology2018
Expression of cleaved caspase-3 predicts good chemotherapy response but poor survival for patients with advanced primary triple-negative breast cancer.
Article in International journal of clinical and experimental pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 12 citations in OpenAlex.
- Association of caspase-3 with thyroid hormone levels in patients with hypothyroidism - A hospital-based study.EJIFCC · 2026Article
- Apoptosis in prostate carcinoma tissue: The role of caspase-3, caspase-1, and alkaline DNase activity.Journal of medical biochemistry · 2025Article
- Prognostic Potential of Apoptosis-Related Biomarker Expression in Triple-Negative Breast Cancers.International journal of molecular sciences · 2025Article
- Article
- Evaluation of cleaved caspase-3 and Ki-67 index on diagnostic biopsy in response to neoadjuvant chemotherapy in the context of post-treatment tumour ypT stage, ypN stage, grade, and molecular subtype.Przeglad menopauzalny = Menopause review · 2024Article
- Combination of Fish Oil and Selenium Enhances Anticancer Efficacy and Targets Multiple Signaling Pathways in Anti-VEGF Agent Treated-TNBC Tumor-Bearing Mice.Marine drugs · 2021Article
- Ground-glass opacity-featured lung adenocarcinoma has no response to chemotherapy.Journal of cancer research and clinical oncology · 2020Article
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
objectiveTo assess cleaved caspase-3 (CC3), Ki-67, and E-cadherin (E-cad) expression in relation to chemotherapy response and prognosis of patients with advanced primary triple-negative breast cancer (TNBC).
methodsCC3 expression was detected immunohistochemically in 67 pre-chemotherapy biopsy samples. Ki67 and E-cad levels were obtained from patients' medical records.
resultsCC3-positivity (N = 32; 47.8%) was associated with a higher first-line chemotherapy overall response rate (ORR; P = 0.028) and second-line chemotherapy clinical benefit rate (CBR; P = 0.033). The Ki-67 high-risk group (N = 51; 76.1%) exhibited a reduced second-line chemotherapy CBR (P = 0.024). The E-cad negative group (N = 25; 37.3%) exhibited a lower first-line chemotherapy ORR (P = 0.044) and CBR (P<0.001), and a lower second-line chemotherapy CBR (P = 0.020). CC3, Ki-67, and E-cad were significant predictors of third-line chemotherapy ORR or CBR. Similar numbers of chemotherapy cycles were completed by the CC3-positive and -negative groups. The Ki-67 high-risk and E-cad negative groups completed fewer second-line chemotherapy cycles (P = 0.038) and fewer first-line chemotherapy cycles, respectively (P = 0.001). Kaplan-Meier analyses identified worse outcomes for the CC3-positive, Ki-67 high-risk, and E-cad negative groups than for their corresponding comparison groups (P<0.05). Multivariate Cox regression analysis identified CC3 expression and an absence of E-cad expression as independent survival factors (P<0.05).
conclusionsOur CC3-positive group exhibited a better chemotherapy response, but a worse prognosis. The Ki-67 high-risk and E-cad negative groups exhibited both a worse chemotherapy response and worse prognosis.
Indexed as
Identifiers
31949833PMC6962992W3027127240What OpenQuestion holds
Registered trials
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