Cargando…

Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis

BACKGROUND: Colon cancer is the second leading cause of death worldwide. Exploring key regulators in colon cancer metastatic progression could lead to better outcomes for patients. METHODS: Initially, the transcriptional profiles of 681 colonrectal cancer (CRC) cases were used to discover signature...

Descripción completa

Detalles Bibliográficos
Autores principales: He, Zhicheng, Lin, Jian, Chen, Cheng, Chen, Yuanzhi, Yang, Shuting, Cai, Xianghai, He, YingYing, Liu, Shubai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663999/
https://www.ncbi.nlm.nih.gov/pubmed/36377223
http://dx.doi.org/10.1002/ctm2.973
_version_ 1784831006396645376
author He, Zhicheng
Lin, Jian
Chen, Cheng
Chen, Yuanzhi
Yang, Shuting
Cai, Xianghai
He, YingYing
Liu, Shubai
author_facet He, Zhicheng
Lin, Jian
Chen, Cheng
Chen, Yuanzhi
Yang, Shuting
Cai, Xianghai
He, YingYing
Liu, Shubai
author_sort He, Zhicheng
collection PubMed
description BACKGROUND: Colon cancer is the second leading cause of death worldwide. Exploring key regulators in colon cancer metastatic progression could lead to better outcomes for patients. METHODS: Initially, the transcriptional profiles of 681 colonrectal cancer (CRC) cases were used to discover signature genes that were significantly correlated with colon cancer metastasis. These signature genes were then validated using another independent 210 CRC cases’ transcriptomics and proteomics profiles, and Kaplan–Meier regression analyses were used to screen the key regulators with patients’ survival. Immunohistochemical staining was used to confirm the biomarkers, and transit knockdown was used to explore their implications on colon cancer cells migration and invasion abilities. The impact on the key signalling molecules in epithelial‐mesenchymal transition (EMT) process that drive tumour metastasis was tested using Western blot. The response to clinical standard therapeutic drugs was compared to clinical prognosis of key regulators using an ROC plotter. RESULTS: Five genes (BGN, THBS2, SPARC, CDH11 and SPP1) were initially identified as potential biomarkers and therapeutic targets of colon cancer metastasis. The most significant signatures associated with colon cancer metastasis were determined to be BGN and THBS2. Furthermore, highly expression of BGN and THBS2 in tumours was linked to a worse survival rate. BGN and THBS2 knockdown significantly reduced colon cancer cells migration and invasion, as well as down‐regulating three EMT‐related proteins (Snail, Vimentin and N‐cadherin), and increasing the proliferation inhibitory effect of 5‐fluorouracil, irinotecan and oxaliplatin treatment. CONCLUSIONS: CRC metastatic progression, EMT phenotypic transition and poor survival time have been linked to BGN and THBS2. They could be utilized as potential diagnostic and therapeutic targets for colon cancer metastatic patients with a better prognosis.
format Online
Article
Text
id pubmed-9663999
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-96639992022-11-16 Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis He, Zhicheng Lin, Jian Chen, Cheng Chen, Yuanzhi Yang, Shuting Cai, Xianghai He, YingYing Liu, Shubai Clin Transl Med Research Articles BACKGROUND: Colon cancer is the second leading cause of death worldwide. Exploring key regulators in colon cancer metastatic progression could lead to better outcomes for patients. METHODS: Initially, the transcriptional profiles of 681 colonrectal cancer (CRC) cases were used to discover signature genes that were significantly correlated with colon cancer metastasis. These signature genes were then validated using another independent 210 CRC cases’ transcriptomics and proteomics profiles, and Kaplan–Meier regression analyses were used to screen the key regulators with patients’ survival. Immunohistochemical staining was used to confirm the biomarkers, and transit knockdown was used to explore their implications on colon cancer cells migration and invasion abilities. The impact on the key signalling molecules in epithelial‐mesenchymal transition (EMT) process that drive tumour metastasis was tested using Western blot. The response to clinical standard therapeutic drugs was compared to clinical prognosis of key regulators using an ROC plotter. RESULTS: Five genes (BGN, THBS2, SPARC, CDH11 and SPP1) were initially identified as potential biomarkers and therapeutic targets of colon cancer metastasis. The most significant signatures associated with colon cancer metastasis were determined to be BGN and THBS2. Furthermore, highly expression of BGN and THBS2 in tumours was linked to a worse survival rate. BGN and THBS2 knockdown significantly reduced colon cancer cells migration and invasion, as well as down‐regulating three EMT‐related proteins (Snail, Vimentin and N‐cadherin), and increasing the proliferation inhibitory effect of 5‐fluorouracil, irinotecan and oxaliplatin treatment. CONCLUSIONS: CRC metastatic progression, EMT phenotypic transition and poor survival time have been linked to BGN and THBS2. They could be utilized as potential diagnostic and therapeutic targets for colon cancer metastatic patients with a better prognosis. John Wiley and Sons Inc. 2022-11-14 /pmc/articles/PMC9663999/ /pubmed/36377223 http://dx.doi.org/10.1002/ctm2.973 Text en © 2022 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
He, Zhicheng
Lin, Jian
Chen, Cheng
Chen, Yuanzhi
Yang, Shuting
Cai, Xianghai
He, YingYing
Liu, Shubai
Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis
title Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis
title_full Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis
title_fullStr Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis
title_full_unstemmed Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis
title_short Identification of BGN and THBS2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis
title_sort identification of bgn and thbs2 as metastasis‐specific biomarkers and poor survival key regulators in human colon cancer by integrated analysis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663999/
https://www.ncbi.nlm.nih.gov/pubmed/36377223
http://dx.doi.org/10.1002/ctm2.973
work_keys_str_mv AT hezhicheng identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis
AT linjian identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis
AT chencheng identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis
AT chenyuanzhi identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis
AT yangshuting identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis
AT caixianghai identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis
AT heyingying identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis
AT liushubai identificationofbgnandthbs2asmetastasisspecificbiomarkersandpoorsurvivalkeyregulatorsinhumancoloncancerbyintegratedanalysis