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KNTC1 as a putative tumor oncogene in pancreatic cancer

PURPOSE: Recent studies have demonstrated that kinetochore-associated protein 1 (KNTC1) plays a significant role in the carcinogenesis of numerous types of cancer. This study aimed to explore the role and possible mechanisms of KNTC1 in the development of pancreatic cancer. METHODS AND RESULTS: We a...

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Autores principales: Liu, Ling, Chen, Hongwei, Chen, Xinan, Yao, Chenjie, Shen, Weimin, Jia, Changku
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314837/
https://www.ncbi.nlm.nih.gov/pubmed/35852618
http://dx.doi.org/10.1007/s00432-022-04146-3
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author Liu, Ling
Chen, Hongwei
Chen, Xinan
Yao, Chenjie
Shen, Weimin
Jia, Changku
author_facet Liu, Ling
Chen, Hongwei
Chen, Xinan
Yao, Chenjie
Shen, Weimin
Jia, Changku
author_sort Liu, Ling
collection PubMed
description PURPOSE: Recent studies have demonstrated that kinetochore-associated protein 1 (KNTC1) plays a significant role in the carcinogenesis of numerous types of cancer. This study aimed to explore the role and possible mechanisms of KNTC1 in the development of pancreatic cancer. METHODS AND RESULTS: We analyzed differentially expressed genes by RNA sequencing in three paired pancreatic cancer and para-cancerous tissue samples and found that the expression of KNTC1 was significantly upregulated in pancreatic cancer. A Cancer and Tumor Gene Map pan-analysis showed that high expression of KNTC1 was related to poor prognosis in 9499 tumor samples. With immunohistochemical staining, we found that the high expression of KNTC1 in pancreatic cancer was related to pathological grade and clinical prognosis. Similarly, RT-PCR results indicated that the expression of KNTC1 was higher in three groups of pancreatic cancer cell lines (BxPC-3, PANC-1, and SW1990) than in normal pancreatic ductal cells. We introduced lentivirus-mediated shRNA targeting KNTC1 into PANC-1 and SW1990 cells and found that KNTC1 knockdown significantly decreased cell growth and increased cell apoptosis compared to the control group cells. Bioinformatic analysis of the cell expression profile revealed that differential genes were mainly enriched in the cell cycle, mitosis, and STAT3 signaling pathways, and co-immunoprecipitation confirmed an interaction between KNTC1 and cell division cycle associated 8. CONCLUSIONS: KNTC1 could be linked to the pathophysiology of pancreatic cancer and may be an early diagnostic marker of cervical precancerous lesions.
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spelling pubmed-103148372023-07-03 KNTC1 as a putative tumor oncogene in pancreatic cancer Liu, Ling Chen, Hongwei Chen, Xinan Yao, Chenjie Shen, Weimin Jia, Changku J Cancer Res Clin Oncol Research PURPOSE: Recent studies have demonstrated that kinetochore-associated protein 1 (KNTC1) plays a significant role in the carcinogenesis of numerous types of cancer. This study aimed to explore the role and possible mechanisms of KNTC1 in the development of pancreatic cancer. METHODS AND RESULTS: We analyzed differentially expressed genes by RNA sequencing in three paired pancreatic cancer and para-cancerous tissue samples and found that the expression of KNTC1 was significantly upregulated in pancreatic cancer. A Cancer and Tumor Gene Map pan-analysis showed that high expression of KNTC1 was related to poor prognosis in 9499 tumor samples. With immunohistochemical staining, we found that the high expression of KNTC1 in pancreatic cancer was related to pathological grade and clinical prognosis. Similarly, RT-PCR results indicated that the expression of KNTC1 was higher in three groups of pancreatic cancer cell lines (BxPC-3, PANC-1, and SW1990) than in normal pancreatic ductal cells. We introduced lentivirus-mediated shRNA targeting KNTC1 into PANC-1 and SW1990 cells and found that KNTC1 knockdown significantly decreased cell growth and increased cell apoptosis compared to the control group cells. Bioinformatic analysis of the cell expression profile revealed that differential genes were mainly enriched in the cell cycle, mitosis, and STAT3 signaling pathways, and co-immunoprecipitation confirmed an interaction between KNTC1 and cell division cycle associated 8. CONCLUSIONS: KNTC1 could be linked to the pathophysiology of pancreatic cancer and may be an early diagnostic marker of cervical precancerous lesions. Springer Berlin Heidelberg 2022-07-19 2023 /pmc/articles/PMC10314837/ /pubmed/35852618 http://dx.doi.org/10.1007/s00432-022-04146-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research
Liu, Ling
Chen, Hongwei
Chen, Xinan
Yao, Chenjie
Shen, Weimin
Jia, Changku
KNTC1 as a putative tumor oncogene in pancreatic cancer
title KNTC1 as a putative tumor oncogene in pancreatic cancer
title_full KNTC1 as a putative tumor oncogene in pancreatic cancer
title_fullStr KNTC1 as a putative tumor oncogene in pancreatic cancer
title_full_unstemmed KNTC1 as a putative tumor oncogene in pancreatic cancer
title_short KNTC1 as a putative tumor oncogene in pancreatic cancer
title_sort kntc1 as a putative tumor oncogene in pancreatic cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10314837/
https://www.ncbi.nlm.nih.gov/pubmed/35852618
http://dx.doi.org/10.1007/s00432-022-04146-3
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