Preprint Review Version 1 Preserved in Portico This version is not peer-reviewed

Tumor Molecular and Microenvironment Characteristics in EBV-Associated Malignancies as Potential Therapeutic Targets: Focus on Gastric Cancer

Version 1 : Received: 6 September 2022 / Approved: 7 September 2022 / Online: 7 September 2022 (03:23:18 CEST)

How to cite: Schuller, A.A.; Abushukair, H.; Cavalcante, L.; Hentzen, S.; Saeed, A.; Saeed, A. Tumor Molecular and Microenvironment Characteristics in EBV-Associated Malignancies as Potential Therapeutic Targets: Focus on Gastric Cancer. Preprints 2022, 2022090096. https://doi.org/10.20944/preprints202209.0096.v1 Schuller, A.A.; Abushukair, H.; Cavalcante, L.; Hentzen, S.; Saeed, A.; Saeed, A. Tumor Molecular and Microenvironment Characteristics in EBV-Associated Malignancies as Potential Therapeutic Targets: Focus on Gastric Cancer. Preprints 2022, 2022090096. https://doi.org/10.20944/preprints202209.0096.v1

Abstract

Although most people are infected with Epstein-Barr Virus (EBV) during their lifetime, only a minority of them develop an EBV-associated malignancy. EBV acts in both direct and indirect ways to transform infected cells into tumor cells. There are multiple ways in which the EBV, host, and tumor environment interact to promote malignant transformation. This paper focuses on some of the mechanisms that EBV uses to transform the tumor microenvironment (TME) of EBV-associated gastric cancer (EBVaGC) for its benefit, including overexpression of IDO1, synergism between H pylori and EBV coinfection, and M1 to M2 switch. In this review, we expand on different modalities and combinatorial approaches to therapeutically target this mechanism.

Keywords

EBV; EBV malignancies; EBV-associated gastric cancer (EBVaGC); Tumor microenvironment (TME); IFN-gamma; IDO1; H pylori; TAMs; M1; M2.

Subject

Medicine and Pharmacology, Oncology and Oncogenics

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