Cargando…

CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2

Lymph node (LN) metastasis affects both the management and prognosis of head and neck squamous cell carcinoma (HNSCC). Here, we explored the relationship between lymphatic metastasis and CEA family member 5 (CEACAM5), including its possible regulatory role in HNSCC. The levels of CEACAM5 in tissues...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Xudong, Li, Yanshi, Pan, Min, Lu, Tao, Wang, Min, Wang, Zhihai, Liu, Chuan, Hu, Guohua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702577/
https://www.ncbi.nlm.nih.gov/pubmed/36377775
http://dx.doi.org/10.1042/CS20220581
_version_ 1784839691552423936
author Wang, Xudong
Li, Yanshi
Pan, Min
Lu, Tao
Wang, Min
Wang, Zhihai
Liu, Chuan
Hu, Guohua
author_facet Wang, Xudong
Li, Yanshi
Pan, Min
Lu, Tao
Wang, Min
Wang, Zhihai
Liu, Chuan
Hu, Guohua
author_sort Wang, Xudong
collection PubMed
description Lymph node (LN) metastasis affects both the management and prognosis of head and neck squamous cell carcinoma (HNSCC). Here, we explored the relationship between lymphatic metastasis and CEA family member 5 (CEACAM5), including its possible regulatory role in HNSCC. The levels of CEACAM5 in tissues from patients with HNSCC, with and without LN metastases, were assessed by transcriptome sequencing. The associations between CEACAM5 and the N stage of LN metastasis in HNSCC were predicted through The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases and a pan-cancer analysis of CEACAM5 expression in 33 common human tumors was conducted. CEACAM5 levels were analyzed in tumor and normal tissue specimens from HNSCC patients and the correlation between CEACAM5 levels and prognosis was evaluated. The influence of CEACAM5 on cell proliferation, invasion, migration, and apoptosis was investigated in HNSCC cell lines, as were the downstream regulatory mechanisms. A mouse model of LN metastasis was constructed. CEACAM5 levels were significantly higher in HNSCC tissue without LN metastasis than in that with LN metastasis. Similar findings were obtained for the clinical specimens. CEACAM5 levels were associated with better clinical prognosis. CEACAM5 was found to inhibit the proliferation and migration and promote the apoptosis of HNSCC cells. A mouse xenograft model showed that CEACAM5 inhibited LN metastasis. In conclusions, CEACAM5 inhibited epithelial–mesenchymal transition (EMT) in HNSCC by reducing murine double minute 2 (MDM2) expression and thereby suppressing LN metastasis. CEACAM5 has potential as both a prognostic marker and a therapeutic target in HNSCC.
format Online
Article
Text
id pubmed-9702577
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Portland Press Ltd.
record_format MEDLINE/PubMed
spelling pubmed-97025772022-12-06 CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2 Wang, Xudong Li, Yanshi Pan, Min Lu, Tao Wang, Min Wang, Zhihai Liu, Chuan Hu, Guohua Clin Sci (Lond) Bioinformatics Lymph node (LN) metastasis affects both the management and prognosis of head and neck squamous cell carcinoma (HNSCC). Here, we explored the relationship between lymphatic metastasis and CEA family member 5 (CEACAM5), including its possible regulatory role in HNSCC. The levels of CEACAM5 in tissues from patients with HNSCC, with and without LN metastases, were assessed by transcriptome sequencing. The associations between CEACAM5 and the N stage of LN metastasis in HNSCC were predicted through The Cancer Genome Atlas (TCGA) and Gene Expression Omnibus (GEO) databases and a pan-cancer analysis of CEACAM5 expression in 33 common human tumors was conducted. CEACAM5 levels were analyzed in tumor and normal tissue specimens from HNSCC patients and the correlation between CEACAM5 levels and prognosis was evaluated. The influence of CEACAM5 on cell proliferation, invasion, migration, and apoptosis was investigated in HNSCC cell lines, as were the downstream regulatory mechanisms. A mouse model of LN metastasis was constructed. CEACAM5 levels were significantly higher in HNSCC tissue without LN metastasis than in that with LN metastasis. Similar findings were obtained for the clinical specimens. CEACAM5 levels were associated with better clinical prognosis. CEACAM5 was found to inhibit the proliferation and migration and promote the apoptosis of HNSCC cells. A mouse xenograft model showed that CEACAM5 inhibited LN metastasis. In conclusions, CEACAM5 inhibited epithelial–mesenchymal transition (EMT) in HNSCC by reducing murine double minute 2 (MDM2) expression and thereby suppressing LN metastasis. CEACAM5 has potential as both a prognostic marker and a therapeutic target in HNSCC. Portland Press Ltd. 2022-11 2022-11-25 /pmc/articles/PMC9702577/ /pubmed/36377775 http://dx.doi.org/10.1042/CS20220581 Text en © 2022 The Author(s). https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Bioinformatics
Wang, Xudong
Li, Yanshi
Pan, Min
Lu, Tao
Wang, Min
Wang, Zhihai
Liu, Chuan
Hu, Guohua
CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2
title CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2
title_full CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2
title_fullStr CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2
title_full_unstemmed CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2
title_short CEACAM5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting MDM2
title_sort ceacam5 inhibits the lymphatic metastasis of head and neck squamous cell carcinoma by regulating epithelial–mesenchymal transition via inhibiting mdm2
topic Bioinformatics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9702577/
https://www.ncbi.nlm.nih.gov/pubmed/36377775
http://dx.doi.org/10.1042/CS20220581
work_keys_str_mv AT wangxudong ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2
AT liyanshi ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2
AT panmin ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2
AT lutao ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2
AT wangmin ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2
AT wangzhihai ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2
AT liuchuan ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2
AT huguohua ceacam5inhibitsthelymphaticmetastasisofheadandnecksquamouscellcarcinomabyregulatingepithelialmesenchymaltransitionviainhibitingmdm2