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Abstract 2242: KRAS mutations suppress the tumor immune microenvironment in colorectal cancer

Authors :
Pariyada Tanjak
Amphun Chaiboonchoe
Tharathorn Suwatthanarak
Onchira Acharayothin
Kullanist Thanormjit
Jantappapa Chanthercrob
Thanawat Suwatthanarak
Bundit Wannasuphaphol
Kemmapon Chumchuen
Bhoom Suktitipat
Somponnat Sampattavanich
Krittiya Korphaisarn
Ananya Pongpaibul
Naravat Poungvarin
Harald Grove
Woramin Riansuwan
Atthaphorn Trakarnsanga
Asada Methasate
Manop Pithukpakorn
Vitoon Chinswangwatanakul
Source :
Cancer Research. 83:2242-2242
Publication Year :
2023
Publisher :
American Association for Cancer Research (AACR), 2023.

Abstract

Background: KRAS mutations (KRASmut) drive tumorigenesis through various signaling pathways that are associated with worse survival in colorectal cancer patients (CRC). Immune evasion is a hallmark of KRAS-driven cancer, but the role of KRASmut in the regulation of the immune response is unclear, particularly in the tumor microenvironment (TME), which often assists cancer cells to thrive and successfully escape immune surveillance. Here, we explore the immunobiological impacts of KRASmut in CRC patients. Methods: A total of 97 fresh frozen tumor samples were collected from each CRC patient with stage I-IV who underwent surgical treatment at the Department of Surgery, Faculty of Medicine Siriraj Hospital between October 2010 and March 2011. First, all patients were identified KRAS mutational status and compared overall survival (OS) with wild-type KRAS (KRASwt). Next, we analyzed the gene expression profiling of KRASmut which was performed using the Nanostring platform. Finally, we performed the biological network analysis focusing on immunological pathways associated with KRASmut using the Ingenuity Pathway Analysis (IPA). Results: We observed KRASmut in 41.24% (n=40) of the total cases. Mutations occurred primarily in exon 2 (total n=36; codon 12, n=28; codon 13, n=8) and rarely in exon 3 (n=4). Patients with KRASmut CRC in exon 2 and exon 3, showed significantly worse OS compared to KRASwt (HR 1.77, 95% CI 1.07-2.93; P Conclusions: Our results suggested that KRASmut activated TGFβ and interrupted pro-inflammatory cytokine to suppress tumor immune microenvironment in CRC. Future studies and clinical trials in patients with CRC with KRASmut should take these transcriptional profiles into account. Citation Format: Pariyada Tanjak, Amphun Chaiboonchoe, Tharathorn Suwatthanarak, Onchira Acharayothin, Kullanist Thanormjit, Jantappapa Chanthercrob, Thanawat Suwatthanarak, Bundit Wannasuphaphol, Kemmapon Chumchuen, Bhoom Suktitipat, Somponnat Sampattavanich, Krittiya Korphaisarn, Ananya Pongpaibul, Naravat Poungvarin, Harald Grove, Woramin Riansuwan, Atthaphorn Trakarnsanga, Asada Methasate, Manop Pithukpakorn, Vitoon Chinswangwatanakul. KRAS mutations suppress the tumor immune microenvironment in colorectal cancer [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2023; Part 1 (Regular and Invited Abstracts); 2023 Apr 14-19; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2023;83(7_Suppl):Abstract nr 2242.

Subjects

Subjects :
Cancer Research
Oncology

Details

ISSN :
15387445
Volume :
83
Database :
OpenAIRE
Journal :
Cancer Research
Accession number :
edsair.doi...........aad1b6e29cbf92be983f3c63e04964ea