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Brunetti, Oronzo

https://orcid.org/0000-0002-7014-6828

Mayo Clinic

Istituto Tumori Bari

Citations 1

Cytotoxic T-Lymphocyte Antigen-4 in Colorectal Cancer: Another Therapeutic Side of Capecitabine
Derakhshani, Afshin , Hashemzadeh, Shahryar, Asadzadeh, Zahra , Shadbad, Mahdi Abdoli , Rasibonab, Farnaz, Safarpour, Hossein , Jafarlou, Vahid , Solimando, Antonio Giovanni , Racanelli, Vito , Najafi, Souzan , Javadrashid, Darya , Brunetti, Oronzo , Silvestris, Nicola , Baradaran, Behzad , Singh, Pankaj Kumar , Brunetti, Oronzo , Silvestris, Nicola , Baradaran, Behzad , Singh, P.

Cancers | May 17, 2021 | Volume: 13 | Issue: 10 | Pages: 2414

10.3390/cancers13102414 Get It

Cytotoxic T lymphocyte antigen-4 (CTLA-4) is an inhibitory immune checkpoint that can be expressed in tumor-infiltrating lymphocytes and colorectal cancer (CRC) cells. This immune checkpoint can attenuate anti-tumoral immune responses and facilitate tumor growth and metastasis. Although capecitabine is an effective chemotherapeutic agent for treating CRC, its effect on the tumoral CTLA-4 expression remains unclear. In the current research, we applied the GSE110224 and GSE25070 datasets to characterize CTLA-4 expression in CRC patients. Then, we analyzed CTLA-4 expression in CRC samples, HT-29, HCT-166, and SW480 cell lines using real-time PCR. Our bioinformatic results have highlighted the overexpression of CTLA-4 in the CRC tissues compared to the adjacent non-tumoral tissues. Our in vitro studies have indicated that SW480 cells can substantially overexpress CTLA-4 compared to HT-29 and HCT 116 cells. In addition, capecitabine can remarkably downregulate the expression of CTLA-4 in SW480 cells. Collectively, capecitabine can inhibit the expression of CTLA-4 in CRC cells and might bridge the immunotherapy approaches with chemotherapy.