Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas

Aim: This study aims to investigate potential associations between the stem cell population and the degree of tumor regression in breast carcinomas treated with neoadjuvant therapy. Settings and Design: The study included 92 patients with breast carcinoma who received neoadjuvant therapy. Tumor regr...

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Main Authors: Zuhal Gucin, Nur Buyukpinarbasili, Melin Ozgun Gecer, Yeliz Emine Ersoy, Haci Mehmet Turk, Seyma Yildiz, Direnc Ozlem Aksoy
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2023-07-01
Series:Indian Journal of Pathology and Microbiology
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Online Access:https://journals.lww.com/10.4103/ijpm.ijpm_1274_21
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author Zuhal Gucin
Nur Buyukpinarbasili
Melin Ozgun Gecer
Yeliz Emine Ersoy
Haci Mehmet Turk
Seyma Yildiz
Direnc Ozlem Aksoy
author_facet Zuhal Gucin
Nur Buyukpinarbasili
Melin Ozgun Gecer
Yeliz Emine Ersoy
Haci Mehmet Turk
Seyma Yildiz
Direnc Ozlem Aksoy
author_sort Zuhal Gucin
collection DOAJ
description Aim: This study aims to investigate potential associations between the stem cell population and the degree of tumor regression in breast carcinomas treated with neoadjuvant therapy. Settings and Design: The study included 92 patients with breast carcinoma who received neoadjuvant therapy. Tumor regression was defined based on Miller and Payne grading system. Patients with grade 1 or 2 regression on a 5-point scale were included in group 1 (n = 37), grade 3 regression in group 2 (n = 32), and grade 4 or 5 regression in group 3 (n = 23). Materials and Methods: Immunohistochemical staining was performed on paraffin block sections of every case using CD44, CD24, CD29, CD133, ID4, and ALDH1 antibodies to detect stem cells. Statistical Analysis Used: IBM Statistical Package for the Social Sciences (SPSS), version 23.0 (IBM Corp., Armonk, NY, USA) software was used for statistical analyses, and a P value less than 0.05 was considered statistically significant. Results: Histologically high-grade tumors are more common in the near-complete/complete response group (P = 0.004). HER2-positive tumors were more common in the complete/near-complete response group (P = 0.054). Tumor cells positive for stem cell markers CD44 and CD24 were more common in the poor response group (P = 0.027 and P = 0.001, respectively). CD29 expression was reduced in the posttreatment residual tumor tissue in the near-complete/complete response group. Conclusion: High CD44 and CD24 expression may be a predictor of poor response/nonresponse to neoadjuvant therapy in breast carcinomas. Background: In recent years, stem cells have been defined as the main cell population responsible for resistance to anticancer therapies.
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spelling doaj-art-a08bf18e088540ffa9c83be415fa30a92025-02-07T13:30:35ZengWolters Kluwer Medknow PublicationsIndian Journal of Pathology and Microbiology0377-49292023-07-0166349550110.4103/ijpm.ijpm_1274_21Stem cell markers: A guide to neoadjuvant therapy in breast carcinomasZuhal GucinNur BuyukpinarbasiliMelin Ozgun GecerYeliz Emine ErsoyHaci Mehmet TurkSeyma YildizDirenc Ozlem AksoyAim: This study aims to investigate potential associations between the stem cell population and the degree of tumor regression in breast carcinomas treated with neoadjuvant therapy. Settings and Design: The study included 92 patients with breast carcinoma who received neoadjuvant therapy. Tumor regression was defined based on Miller and Payne grading system. Patients with grade 1 or 2 regression on a 5-point scale were included in group 1 (n = 37), grade 3 regression in group 2 (n = 32), and grade 4 or 5 regression in group 3 (n = 23). Materials and Methods: Immunohistochemical staining was performed on paraffin block sections of every case using CD44, CD24, CD29, CD133, ID4, and ALDH1 antibodies to detect stem cells. Statistical Analysis Used: IBM Statistical Package for the Social Sciences (SPSS), version 23.0 (IBM Corp., Armonk, NY, USA) software was used for statistical analyses, and a P value less than 0.05 was considered statistically significant. Results: Histologically high-grade tumors are more common in the near-complete/complete response group (P = 0.004). HER2-positive tumors were more common in the complete/near-complete response group (P = 0.054). Tumor cells positive for stem cell markers CD44 and CD24 were more common in the poor response group (P = 0.027 and P = 0.001, respectively). CD29 expression was reduced in the posttreatment residual tumor tissue in the near-complete/complete response group. Conclusion: High CD44 and CD24 expression may be a predictor of poor response/nonresponse to neoadjuvant therapy in breast carcinomas. Background: In recent years, stem cells have been defined as the main cell population responsible for resistance to anticancer therapies.https://journals.lww.com/10.4103/ijpm.ijpm_1274_21breast cancersneoadjuvant treatmentstem cell markersstem cellstumor regression grade
spellingShingle Zuhal Gucin
Nur Buyukpinarbasili
Melin Ozgun Gecer
Yeliz Emine Ersoy
Haci Mehmet Turk
Seyma Yildiz
Direnc Ozlem Aksoy
Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas
Indian Journal of Pathology and Microbiology
breast cancers
neoadjuvant treatment
stem cell markers
stem cells
tumor regression grade
title Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas
title_full Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas
title_fullStr Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas
title_full_unstemmed Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas
title_short Stem cell markers: A guide to neoadjuvant therapy in breast carcinomas
title_sort stem cell markers a guide to neoadjuvant therapy in breast carcinomas
topic breast cancers
neoadjuvant treatment
stem cell markers
stem cells
tumor regression grade
url https://journals.lww.com/10.4103/ijpm.ijpm_1274_21
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AT nurbuyukpinarbasili stemcellmarkersaguidetoneoadjuvanttherapyinbreastcarcinomas
AT melinozgungecer stemcellmarkersaguidetoneoadjuvanttherapyinbreastcarcinomas
AT yelizemineersoy stemcellmarkersaguidetoneoadjuvanttherapyinbreastcarcinomas
AT hacimehmetturk stemcellmarkersaguidetoneoadjuvanttherapyinbreastcarcinomas
AT seymayildiz stemcellmarkersaguidetoneoadjuvanttherapyinbreastcarcinomas
AT direncozlemaksoy stemcellmarkersaguidetoneoadjuvanttherapyinbreastcarcinomas