Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers

Background Cervical cancer is the most common gynecological cancer, encompassing cervical squamous cell carcinoma, adenocarcinoma, and other epithelial tumors. There are many diagnostic methods to detect cervical cancers but no precision screening tool for cervical adenocarcinoma at present. Materia...

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Main Authors: Zhifang Ma, Jie Chen, Ting Luan, Chengzhuo Chu, Wangfei Wu, Yichao Zhu, Yun Gu
Format: Article
Language:English
Published: PeerJ Inc. 2020-07-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/9527.pdf
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author Zhifang Ma
Jie Chen
Ting Luan
Chengzhuo Chu
Wangfei Wu
Yichao Zhu
Yun Gu
author_facet Zhifang Ma
Jie Chen
Ting Luan
Chengzhuo Chu
Wangfei Wu
Yichao Zhu
Yun Gu
author_sort Zhifang Ma
collection DOAJ
description Background Cervical cancer is the most common gynecological cancer, encompassing cervical squamous cell carcinoma, adenocarcinoma, and other epithelial tumors. There are many diagnostic methods to detect cervical cancers but no precision screening tool for cervical adenocarcinoma at present. Material and methods The cervical mucus from three normal cervices (Ctrl), three endocervical adenocarcinoma (EA), and three cervical adenocarcinoma in situ (AIS) was collected for proteomic analysis. The proteins were screened using liquid chromatography-mass spectrometry analysis (LC-MS). The biological function of the differently expressed proteins were predicted by Gene Ontology (GO). Results A total of 711 proteins were identified, including 237 differently expressed proteins identified in EA/Ctrl comparison, 256 differently expressed proteins identified in AIS/Ctrl comparison, and 242 differently expressed proteins identified in AIS/EA comparison (up-regulate ≥ 1.5 or down-regulate ≤ 0.67). Functional annotation was performed using GO analysis on 1,056 differently expressed proteins to identify those that may impact cervical cancer, such as heme protein myeloperoxidase, which is involved in the immune process, and APOA1, which is associated with lipid metabolism. Conclusion We used proteomic analysis to screen out differently expressed proteins from normal cervical mucus and cervical adenocarcinoma mucus samples. These differently expressed proteins may be potential biomarkers for the diagnosis and treatment of cervical adenocarcinoma but require additional study.
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spelling doaj.art-db57ea4a89b84ebb9f3ed6382993a75c2023-12-03T09:45:53ZengPeerJ Inc.PeerJ2167-83592020-07-018e952710.7717/peerj.9527Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkersZhifang Ma0Jie Chen1Ting Luan2Chengzhuo Chu3Wangfei Wu4Yichao Zhu5Yun Gu6Department of Pathology, Women’s Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, ChinaDepartment of Gynecology, Women’s Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, ChinaDepartment of Gynecology, Women’s Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, ChinaDepartment of Pathology, Women’s Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, ChinaDepartment of Pathology, Women’s Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, ChinaDepartment of Physiology, Nanjing Medical University, Nanjing, ChinaDepartment of Pathology, Women’s Hospital of Nanjing Medical University, Nanjing Maternity and Child Health Care Hospital, Nanjing, ChinaBackground Cervical cancer is the most common gynecological cancer, encompassing cervical squamous cell carcinoma, adenocarcinoma, and other epithelial tumors. There are many diagnostic methods to detect cervical cancers but no precision screening tool for cervical adenocarcinoma at present. Material and methods The cervical mucus from three normal cervices (Ctrl), three endocervical adenocarcinoma (EA), and three cervical adenocarcinoma in situ (AIS) was collected for proteomic analysis. The proteins were screened using liquid chromatography-mass spectrometry analysis (LC-MS). The biological function of the differently expressed proteins were predicted by Gene Ontology (GO). Results A total of 711 proteins were identified, including 237 differently expressed proteins identified in EA/Ctrl comparison, 256 differently expressed proteins identified in AIS/Ctrl comparison, and 242 differently expressed proteins identified in AIS/EA comparison (up-regulate ≥ 1.5 or down-regulate ≤ 0.67). Functional annotation was performed using GO analysis on 1,056 differently expressed proteins to identify those that may impact cervical cancer, such as heme protein myeloperoxidase, which is involved in the immune process, and APOA1, which is associated with lipid metabolism. Conclusion We used proteomic analysis to screen out differently expressed proteins from normal cervical mucus and cervical adenocarcinoma mucus samples. These differently expressed proteins may be potential biomarkers for the diagnosis and treatment of cervical adenocarcinoma but require additional study.https://peerj.com/articles/9527.pdfCervical adenocarcinomaMucusProteomicsBiomarkers
spellingShingle Zhifang Ma
Jie Chen
Ting Luan
Chengzhuo Chu
Wangfei Wu
Yichao Zhu
Yun Gu
Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers
PeerJ
Cervical adenocarcinoma
Mucus
Proteomics
Biomarkers
title Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers
title_full Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers
title_fullStr Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers
title_full_unstemmed Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers
title_short Proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers
title_sort proteomic analysis of human cervical adenocarcinoma mucus to identify potential protein biomarkers
topic Cervical adenocarcinoma
Mucus
Proteomics
Biomarkers
url https://peerj.com/articles/9527.pdf
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