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pmid:37904433

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

Tao Chen · Yunqian Chu · Haiyuan Xu · Hanjue Dai · Yuxi Zhou · Haiwei Du · Wenyu Zhu

Medicine · 2023 doi:10.1097/MD.0000000000035491

Paper

complete

Experiment

complete

Data

partial

Analysis

partial

Execution

absent

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title
Kinesin superfamily member KIFC2 as an independent prognostic biomarker of colon adenocarcinoma associated with poor immune response.
doi
10.1097/MD.0000000000035491
pmid
37904433
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[0]
Tao Chen
[1]
Yunqian Chu
[2]
Haiyuan Xu
[3]
Hanjue Dai
[4]
Yuxi Zhou
[5]
Haiwei Du
[6]
Wenyu Zhu
journal
Medicine
year
2023
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.
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Kaplan–Meier method was applied for survival analysis and the log-rank test was used to estimate statistical significance. Multivariate Cox regression analysis was used to screen potential prognostic factors.
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Kaplan–Meier method was applied for survival analysis and the log-rank test was used to estimate statistical significance. Multivariate Cox regression analysis was used to screen potential prognostic factors.
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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.
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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.
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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.
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title
Metastasis Gene Expression Profile Predicts Recurrence and Death in Colon Cancer Patients (Moffitt Samples)
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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.", "claims": [{"id": "claim-method", "statement": "Kaplan–Meier method was applied for survival analysis and the log-rank test was used to estimate statistical significance. 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