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Obtaining Cancer Stem Cell Spheres from Gynecological and Breast Cancer Tumors
Published on: March 1, 2020
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Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas
Zuhal Gucin1, Nur Buyukpinarbasili2, Melin Ozgun Gecer1
1Department of Pathology, Faculty of Medicine, Bezmialem Vakif University, Istanbul, Turkey.
Indian Journal of Pathology & Microbiology
|August 2, 2023
Summary
High expression of CD44 and CD24 stem cell markers in breast cancer may predict poor response to neoadjuvant therapy. This finding suggests these markers could indicate treatment resistance in breast carcinomas.
Area of Science:
- Oncology
- Cancer Biology
- Translational Research
Background:
- Stem cells are increasingly recognized as key drivers of resistance to anticancer therapies.
- Understanding the role of stem cell populations in treatment response is crucial for improving breast cancer outcomes.
Purpose of the Study:
- To investigate the association between stem cell markers and tumor regression in breast carcinomas following neoadjuvant therapy.
- To identify potential stem cell-based predictors of treatment response in breast cancer.
Main Methods:
- Analysis of 92 breast carcinoma patients undergoing neoadjuvant therapy.
- Tumor regression assessment using the Miller and Payne grading system.
- Immunohistochemical detection of stem cell markers (CD44, CD24, CD29, CD133, ID4, ALDH1) in tumor tissues.
Main Results:
- High-grade tumors and HER2-positive status were more frequent in patients with near-complete/complete response.
- Increased expression of CD44 and CD24 was significantly associated with poor response to therapy (P = 0.027 and P = 0.001, respectively).
- CD29 expression was reduced in residual tumors of patients with a near-complete/complete response.
Conclusions:
- Elevated CD44 and CD24 expression may serve as predictive biomarkers for non-response to neoadjuvant therapy in breast cancer.
- Targeting CD44 and CD24 pathways could be a potential strategy to overcome treatment resistance in breast carcinomas.

