Kinesin superfamily member KIFC2 as an independent prognostic biomarker of colon adenocarcinoma associated with poor immune response

Author:

Chen Tao1,Chu Yunqian2,Xu Haiyuan3,Dai Hanjue2,Zhou Yuxi4,Du Haiwei4,Zhu Wenyu2ORCID

Affiliation:

1. Department of Gastrointestinal Surgery, The Affiliated Changzhou No.2 People’s Hospital with Nanjing Medical University, Changzhou, Jiangsu, China

2. Cancer Center, The Affiliated Changzhou No. 2 People’s Hospital with Nanjing Medical University, Changzhou, Jiangsu, China

3. Department of Medical Oncology, Kunshan First People’s Hospital Affiliated to Jiangsu University, Kunshan, Jiangsu, China

4. Burning Rock Biotech, Guangzhou, China.

Abstract

Clinical outcomes of colon adenocarcinoma (COAD) exhibit heterogeneity among different patients, highlighting the need for novel prognostic biomarkers. Kinesin superfamily members have been shown to play a crucial role in tumors and can predict cancer diagnosis and prognosis. However, the role of kinesin family member C2 (KIFC2) in tumors, particularly its prognostic value in COAD, remains poorly understood. Our bioinformatics analysis of the cancer genome atlas and GEO databases revealed significantly higher expression of KIFC2 in COAD, correlating with a worse prognosis in the cancer genome atlas-COAD and GSE17536 cohorts. Additionally, differentially expressed genes in COAD were enriched in immune-related pathways, and patients with higher KIFC2 expression showed fewer activated CD4 + T cells. These findings suggest KIFC2 as a potential prognostic biomarker for COAD, warranting further validation in clinical studies.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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