AI Article Synopsis

  • Gastrointestinal tumors are complex cancers typically treated with surgery, chemotherapy, and radiotherapy, but new advancements in immunotherapy are being explored.
  • A promising target for this new approach is VISTA, a protein that suppresses T-cell activation and may help improve immune responses against tumors.
  • While initial studies indicate VISTA could be a viable target in combination therapies, further research is needed to fully understand its mechanisms and optimize its clinical application.

Article Abstract

While gastrointestinal tumors remain a multifactorial and prevalent group of malignancies commonly treated surgically in combination with chemotherapy and radiotherapy, advancements regarding immunotherapeutic approaches continue to occur. Entering a new era of immunotherapy focused on overcoming resistance to preceding therapies caused the emergence of new therapeutic strategies. A promising solution surfaces with a V-domain Ig suppressor of T-cell activation (VISTA), a negative regulator of a T-cell function expressed in hematopoietic cells. Due to VISTA's ability to act as both a ligand and a receptor, several therapeutic approaches can be potentially developed. A broad expression of VISTA was discovered on various tumor-growth-controlling cells, which proved to increase in specific tumor microenvironment (TME) conditions, thus serving as a rationale behind the development of new VISTA-targeting. Nevertheless, VISTA's ligands and signaling pathways are still not fully understood. The uncertain results of clinical trials suggest the need for future examining inhibitor agents for VISTA and implicating a double immunotherapeutic blockade. However, more research is needed before the breakthrough can be achieved. This review discusses perspectives and novel approaches presented in the current literature. Based on the results of the ongoing studies, VISTA might be considered a potential target in combined therapy, especially for treating gastrointestinal malignancies.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10297928PMC
http://dx.doi.org/10.3390/ijms24129945DOI Listing

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