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ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer

PURPOSE: To develop new and effective biomarkers for the diagnosis of colorectal cancer (CRC). EXPERIMENTAL DESIGN: The serum expression of ITGB4 (49 CRC and 367 HC) was detected by enzyme‐linked immunosorbent assay (ELISA), and its diagnostic value was analyzed using the receiver operating characte...

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Autores principales: Jiang, Xia, Wang, Jia, Wang, Mengyu, Xuan, Mingda, Han, Shuangshuang, Li, Chao, Li, Meng, Sun, Xiao‐Feng, Yu, Weifang, Zhao, Zengren
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495272/
https://www.ncbi.nlm.nih.gov/pubmed/34414684
http://dx.doi.org/10.1002/cam4.4216
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author Jiang, Xia
Wang, Jia
Wang, Mengyu
Xuan, Mingda
Han, Shuangshuang
Li, Chao
Li, Meng
Sun, Xiao‐Feng
Yu, Weifang
Zhao, Zengren
author_facet Jiang, Xia
Wang, Jia
Wang, Mengyu
Xuan, Mingda
Han, Shuangshuang
Li, Chao
Li, Meng
Sun, Xiao‐Feng
Yu, Weifang
Zhao, Zengren
author_sort Jiang, Xia
collection PubMed
description PURPOSE: To develop new and effective biomarkers for the diagnosis of colorectal cancer (CRC). EXPERIMENTAL DESIGN: The serum expression of ITGB4 (49 CRC and 367 HC) was detected by enzyme‐linked immunosorbent assay (ELISA), and its diagnostic value was analyzed using the receiver operating characteristic (ROC) curve. The sensitivity and specificity of ITGB4 in CRC diagnosis were calculated through statistical analysis. The optimal clinical cutoff value was calculated using the Youden index, and diagnostic efficacy was analyzed in a larger serum sample (98 CRC and 1631 non‐CRC). The expression of ITGB4 was measured by CyTOF (cell experimental technology) at the single‐cell level, and characteristics were analyzed using viSNE and SPADE TREE. RESULTS: Serum ITGB4 and CEA levels were significantly higher in CRC patients than in HC and non‐CRC patients. The use of serum ITGB4 levels for the diagnosis of CRC has a high sensitivity (79%) but not high specificity when the clinical cutoff value was 0.70 ng/mL. However, the optimal cutoff value was 1.6 ng/mL with 86.2% specificity and 52.0% sensitivity, and the diagnostic efficacy was greatly improved with high specificity (82.0%) and sensitivity (71.4%) when combined with CEA. ITGB4 expression characteristics were measured and related to the expression of EpCAM, Ck8/18, and perforin at the single‐cell level. Single‐cell analysis showed that cell clusters with low expression of CK8/18 and ITGB4 were more sensitive to 5FU and radiotherapy (RT). CONCLUSIONS: ITGB4 is an effective diagnostic serum biomarker and a potential therapeutic target for CRC.
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spelling pubmed-84952722021-10-08 ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer Jiang, Xia Wang, Jia Wang, Mengyu Xuan, Mingda Han, Shuangshuang Li, Chao Li, Meng Sun, Xiao‐Feng Yu, Weifang Zhao, Zengren Cancer Med Cancer Biology PURPOSE: To develop new and effective biomarkers for the diagnosis of colorectal cancer (CRC). EXPERIMENTAL DESIGN: The serum expression of ITGB4 (49 CRC and 367 HC) was detected by enzyme‐linked immunosorbent assay (ELISA), and its diagnostic value was analyzed using the receiver operating characteristic (ROC) curve. The sensitivity and specificity of ITGB4 in CRC diagnosis were calculated through statistical analysis. The optimal clinical cutoff value was calculated using the Youden index, and diagnostic efficacy was analyzed in a larger serum sample (98 CRC and 1631 non‐CRC). The expression of ITGB4 was measured by CyTOF (cell experimental technology) at the single‐cell level, and characteristics were analyzed using viSNE and SPADE TREE. RESULTS: Serum ITGB4 and CEA levels were significantly higher in CRC patients than in HC and non‐CRC patients. The use of serum ITGB4 levels for the diagnosis of CRC has a high sensitivity (79%) but not high specificity when the clinical cutoff value was 0.70 ng/mL. However, the optimal cutoff value was 1.6 ng/mL with 86.2% specificity and 52.0% sensitivity, and the diagnostic efficacy was greatly improved with high specificity (82.0%) and sensitivity (71.4%) when combined with CEA. ITGB4 expression characteristics were measured and related to the expression of EpCAM, Ck8/18, and perforin at the single‐cell level. Single‐cell analysis showed that cell clusters with low expression of CK8/18 and ITGB4 were more sensitive to 5FU and radiotherapy (RT). CONCLUSIONS: ITGB4 is an effective diagnostic serum biomarker and a potential therapeutic target for CRC. John Wiley and Sons Inc. 2021-08-20 /pmc/articles/PMC8495272/ /pubmed/34414684 http://dx.doi.org/10.1002/cam4.4216 Text en © 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. 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 Cancer Biology
Jiang, Xia
Wang, Jia
Wang, Mengyu
Xuan, Mingda
Han, Shuangshuang
Li, Chao
Li, Meng
Sun, Xiao‐Feng
Yu, Weifang
Zhao, Zengren
ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer
title ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer
title_full ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer
title_fullStr ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer
title_full_unstemmed ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer
title_short ITGB4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer
title_sort itgb4 as a novel serum diagnosis biomarker and potential therapeutic target for colorectal cancer
topic Cancer Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8495272/
https://www.ncbi.nlm.nih.gov/pubmed/34414684
http://dx.doi.org/10.1002/cam4.4216
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