Expression of kinesin family member C1 in pancreatic ductal adenocarcinoma affects tumor progression and stemness

Pancreatic ductal adenocarcinoma (PDAC) is an aggressive cancer and the third leading cause of cancer-related deaths. Therefore, there is an urgent need for a novel molecular target for the treatment of PDAC. Kinesin family member C1 (KIFC1) belongs to the kinesin superfamily proteins and has been r...

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Veröffentlicht in:Pathology, research and practice research and practice, 2023-01, Vol.241, p.154277-154277, Article 154277
Hauptverfasser: Ishikawa, Akira, Fujii, Hiroki, Fukui, Takafumi, Kido, Aya, Katsuya, Narutaka, Sentani, Kazuhiro, Kuraoka, Kazuya, Tazuma, Sho, Sudo, Takeshi, Serikawa, Masahiro, Oka, Shiro, Oue, Naohide
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Sprache:eng
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Zusammenfassung:Pancreatic ductal adenocarcinoma (PDAC) is an aggressive cancer and the third leading cause of cancer-related deaths. Therefore, there is an urgent need for a novel molecular target for the treatment of PDAC. Kinesin family member C1 (KIFC1) belongs to the kinesin superfamily proteins and has been reported to be involved in the pathogenesis of a wide variety of carcinomas. However, the role of KIFC1 in PDAC remains unknown. This study aimed to analyze the expression and biological function of KIFC1 in PDAC. Immunohistochemically, KIFC1 was found in 37 of 81 PDAC cases (46%). A high expression of KIFC1 was significantly related to tumor size (p = 0.023) and poor overall survival (p = 0.011). Univariate and multivariate analysis indicated that KIFC1 expression was a prognostic factor in PDAC cases. As for cancer stem cell markers, KIFC1 expression tended to co-express significantly with CD44 (p 
ISSN:0344-0338
1618-0631
DOI:10.1016/j.prp.2022.154277