An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human Tumors

Kinesin family member C1 (KIFC1) is a minus-end-directed motor protein that is critically involved in microtubule crosslinking and spindle formation. KIFC1 is essential for supernumerary centrosomes, and it is associated with the initiation and progression of cancers. In the present study, we initia...

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Main Authors: Hao Wu, Yingjuan Duan, Siming Gong, Qiang Zhu, Xuanyou Liu, Zhenguo Liu
Format: Article
Language:English
Published: MDPI AG 2022-03-01
Series:Biomedicines
Subjects:
Online Access:https://www.mdpi.com/2227-9059/10/3/637
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author Hao Wu
Yingjuan Duan
Siming Gong
Qiang Zhu
Xuanyou Liu
Zhenguo Liu
author_facet Hao Wu
Yingjuan Duan
Siming Gong
Qiang Zhu
Xuanyou Liu
Zhenguo Liu
author_sort Hao Wu
collection DOAJ
description Kinesin family member C1 (KIFC1) is a minus-end-directed motor protein that is critically involved in microtubule crosslinking and spindle formation. KIFC1 is essential for supernumerary centrosomes, and it is associated with the initiation and progression of cancers. In the present study, we initially reviewed the The Cancer Genome Atlas database and observed that <i>KIFC1</i> is abundantly expressed in most types of tumors. We then analyzed the gene alteration profiles, protein expressions, prognoses, and immune reactivities of KIFC1 in more than 10,000 samples from several well-established databases. In addition, we conducted a gene set enrichment analysis to investigate the potential mechanisms for the roles of <i>KIFC1</i> in carcinogenesis. The pan-cancer analysis of KIFC1 demonstrates significant statistical correlations of the KIFC1 expression with the clinical prognoses, the oncogenic signature gene sets, the myeloid-derived suppressor cell infiltration, the ImmunoScore, the immune checkpoints, the microsatellite instabilities, and the tumor mutational burdens across multiple tumors. These data may provide important information on the understanding of the role and mechanisms of KIFC1 in carcinogenesis and immunotherapy, as well as on the clinical progression of a variety of cancers.
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spelling doaj.art-3619acee362f483c933e832eeb01ac0f2023-11-24T00:33:09ZengMDPI AGBiomedicines2227-90592022-03-0110363710.3390/biomedicines10030637An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human TumorsHao Wu0Yingjuan Duan1Siming Gong2Qiang Zhu3Xuanyou Liu4Zhenguo Liu5Center for Precision Medicine and Division of Cardiovascular Medicine, University of Missouri School of Medicine, Columbia, MO 65212, USAFaculty of Chemistry and Mineralogy, University of Leipzig, 04103 Leipzig, GermanyInstitute of Anatomy, University of Leipzig, 04103 Leipzig, GermanyCenter for Precision Medicine and Division of Cardiovascular Medicine, University of Missouri School of Medicine, Columbia, MO 65212, USACenter for Precision Medicine and Division of Cardiovascular Medicine, University of Missouri School of Medicine, Columbia, MO 65212, USACenter for Precision Medicine and Division of Cardiovascular Medicine, University of Missouri School of Medicine, Columbia, MO 65212, USAKinesin family member C1 (KIFC1) is a minus-end-directed motor protein that is critically involved in microtubule crosslinking and spindle formation. KIFC1 is essential for supernumerary centrosomes, and it is associated with the initiation and progression of cancers. In the present study, we initially reviewed the The Cancer Genome Atlas database and observed that <i>KIFC1</i> is abundantly expressed in most types of tumors. We then analyzed the gene alteration profiles, protein expressions, prognoses, and immune reactivities of KIFC1 in more than 10,000 samples from several well-established databases. In addition, we conducted a gene set enrichment analysis to investigate the potential mechanisms for the roles of <i>KIFC1</i> in carcinogenesis. The pan-cancer analysis of KIFC1 demonstrates significant statistical correlations of the KIFC1 expression with the clinical prognoses, the oncogenic signature gene sets, the myeloid-derived suppressor cell infiltration, the ImmunoScore, the immune checkpoints, the microsatellite instabilities, and the tumor mutational burdens across multiple tumors. These data may provide important information on the understanding of the role and mechanisms of KIFC1 in carcinogenesis and immunotherapy, as well as on the clinical progression of a variety of cancers.https://www.mdpi.com/2227-9059/10/3/637KIFC1pan cancerprognosisMDSCsimmunotherapy
spellingShingle Hao Wu
Yingjuan Duan
Siming Gong
Qiang Zhu
Xuanyou Liu
Zhenguo Liu
An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human Tumors
Biomedicines
KIFC1
pan cancer
prognosis
MDSCs
immunotherapy
title An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human Tumors
title_full An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human Tumors
title_fullStr An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human Tumors
title_full_unstemmed An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human Tumors
title_short An Integrative Pan-Cancer Analysis of Kinesin Family Member C1 (KIFC1) in Human Tumors
title_sort integrative pan cancer analysis of kinesin family member c1 kifc1 in human tumors
topic KIFC1
pan cancer
prognosis
MDSCs
immunotherapy
url https://www.mdpi.com/2227-9059/10/3/637
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