Ismail Saygin, Zeynep Turkmen Usta, Ahmet Akbas, Zeynep Sagnak Yilmaz, Gizem Teoman, Sevdegul Aydin Mungan
{"title":"The Status of CTLA-4 in Colorectal Carcinomas; Relationship with Prognostic Parameters, Her-2 and MMR Proteins.","authors":"Ismail Saygin, Zeynep Turkmen Usta, Ahmet Akbas, Zeynep Sagnak Yilmaz, Gizem Teoman, Sevdegul Aydin Mungan","doi":"10.5146/tjpath.2026.13533","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Colorectal cancer (CRC) is the third most common type of cancer worldwide and the fourth most common cause of cancer-related deaths. Innovative approaches like immunotherapy are necessary for treatment-resistant patients with a poor prognosis. This study aimed to investigate the status of CTLA-4, one of the immune checkpoint molecules, in CRCs.</p><p><strong>Material and methods: </strong>A total of 183 resected CRCs were analyzed retrospectively. Immunohistochemical staining was conducted using an anti-CTLA-4 antibody. The relationship between CTLA-4 and prognostic parameters, such as HER2 and microsatellite instability (MSI), was investigated.</p><p><strong>Results: </strong>One hundred and four of the cases were male, and 79 were female. One hundred fifty-nine of the cases were conventional adenocarcinomas, while 24 were mucinous adenocarcinomas. In 53 of the cases (29%), CTLA-4 showed less than 1% staining in the immune cells, classifying it as negative. In the remaining cases (71%), varying degrees of immune cell staining with CTLA-4 were observed. Conventional adenocarcinomas exhibited a higher expression of CTLA-4 compared to mucinous carcinomas. No statistically significant correlation was found between MSI status and CTLA-4 immune cell staining (p = 0.572). CTLA-4 positivity decreased significantly as tumor diameter decreased (p = 0.029). There was no correlation between the CTLA-4 immunostaining and median survival time.</p><p><strong>Conclusion: </strong>CTLA-4 expression was detected in 71% of CRCs. CTLA-4 positivity significantly decreased as tumor diameter decreased. There was no significant association between CTLA-4 expression and MSI or other prognostic parameters. Additionally, no significant correlation was found between CTLA-4 expression and median survival time. Nevertheless, the presence of CTLA-4 expression in the majority of CRCs is promising for anti-CTLA-4 therapy.</p>","PeriodicalId":45415,"journal":{"name":"Turkish Journal of Pathology","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2026-06-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Turkish Journal of Pathology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5146/tjpath.2026.13533","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PATHOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: Colorectal cancer (CRC) is the third most common type of cancer worldwide and the fourth most common cause of cancer-related deaths. Innovative approaches like immunotherapy are necessary for treatment-resistant patients with a poor prognosis. This study aimed to investigate the status of CTLA-4, one of the immune checkpoint molecules, in CRCs.
Material and methods: A total of 183 resected CRCs were analyzed retrospectively. Immunohistochemical staining was conducted using an anti-CTLA-4 antibody. The relationship between CTLA-4 and prognostic parameters, such as HER2 and microsatellite instability (MSI), was investigated.
Results: One hundred and four of the cases were male, and 79 were female. One hundred fifty-nine of the cases were conventional adenocarcinomas, while 24 were mucinous adenocarcinomas. In 53 of the cases (29%), CTLA-4 showed less than 1% staining in the immune cells, classifying it as negative. In the remaining cases (71%), varying degrees of immune cell staining with CTLA-4 were observed. Conventional adenocarcinomas exhibited a higher expression of CTLA-4 compared to mucinous carcinomas. No statistically significant correlation was found between MSI status and CTLA-4 immune cell staining (p = 0.572). CTLA-4 positivity decreased significantly as tumor diameter decreased (p = 0.029). There was no correlation between the CTLA-4 immunostaining and median survival time.
Conclusion: CTLA-4 expression was detected in 71% of CRCs. CTLA-4 positivity significantly decreased as tumor diameter decreased. There was no significant association between CTLA-4 expression and MSI or other prognostic parameters. Additionally, no significant correlation was found between CTLA-4 expression and median survival time. Nevertheless, the presence of CTLA-4 expression in the majority of CRCs is promising for anti-CTLA-4 therapy.