HIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells

HIG1 domain family member 1A (Higd-1a) interacts with dynamin-like 120 kDa protein to maintain the morphological and functional integrity of the mitochondria and thus plays an important role in the progression of malignant tumors. Higd-1a promotes the proliferation of pancreatic cancer cells and the...

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Autores principales: Zhenyu Xu, Junjie Sun, Yang Chen, Ting Zhang, Yan Qin, Dong Hua
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Publicado: Taylor & Francis Group 2021
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spelling oai:doaj.org-article:9cd6e79feedd483f957b4573ab8890152021-11-26T11:19:49ZHIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells2165-59792165-598710.1080/21655979.2021.1999368https://doaj.org/article/9cd6e79feedd483f957b4573ab8890152021-11-01T00:00:00Zhttp://dx.doi.org/10.1080/21655979.2021.1999368https://doaj.org/toc/2165-5979https://doaj.org/toc/2165-5987HIG1 domain family member 1A (Higd-1a) interacts with dynamin-like 120 kDa protein to maintain the morphological and functional integrity of the mitochondria and thus plays an important role in the progression of malignant tumors. Higd-1a promotes the proliferation of pancreatic cancer cells and the growth of pancreatic cancer; however, no similar observations have been reported for colorectal cancer (CRC). This study, therefore, aimed to verify the role of Higd-1a in CRC. We downloaded data from the Genotype-Tissue Expression (GTEX) and The Cancer Genome Atlas (TCGA) databases and identified an association between Higd-1a levels in colon adenocarcinoma (COAD) tissues and poor survival using Kaplan–Meier curves. Subsequently, we overexpressed Higd-1a in the human COAD cell line HCT-8, knocked down Higd-1a expression in SW480 cells, and evaluated the effects via quantitative PCR (qPCR) and western blotting. MTT assays, colony formation assay, cell cycle analysis, annexin V-FITC/PI, wound-healing analysis, and transwell assay were used to test cell proliferation, formation of cell colonies, cell cycle progression, migration, invasiveness, and apoptosis. Higd-1a has low transcription levels in COAD tissue and suggests a poor prognosis. Higd-1a overexpression in HCT-8 cells weakened cell proliferation, formation of cell colonies, cell cycle progression, migration ability, and invasiveness, and increased apoptosis. Moreover, the decrease of Higd-1a in SW480 cells induced cell proliferation, formation of cell colonies, cell cycle progression, migration, and invasion, and inhibited apoptosis. Higd-1a is underexpressed in COAD cells and its overexpression impaired the proliferation, migration, and invasiveness of COAD cells.Zhenyu XuJunjie SunYang ChenTing ZhangYan QinDong HuaTaylor & Francis Grouparticlehig1 domain family member 1acolorectal cancerproliferationBiotechnologyTP248.13-248.65ENBioengineered, Vol 0, Iss 0 (2021)
institution DOAJ
collection DOAJ
language EN
topic hig1 domain family member 1a
colorectal cancer
proliferation
Biotechnology
TP248.13-248.65
spellingShingle hig1 domain family member 1a
colorectal cancer
proliferation
Biotechnology
TP248.13-248.65
Zhenyu Xu
Junjie Sun
Yang Chen
Ting Zhang
Yan Qin
Dong Hua
HIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells
description HIG1 domain family member 1A (Higd-1a) interacts with dynamin-like 120 kDa protein to maintain the morphological and functional integrity of the mitochondria and thus plays an important role in the progression of malignant tumors. Higd-1a promotes the proliferation of pancreatic cancer cells and the growth of pancreatic cancer; however, no similar observations have been reported for colorectal cancer (CRC). This study, therefore, aimed to verify the role of Higd-1a in CRC. We downloaded data from the Genotype-Tissue Expression (GTEX) and The Cancer Genome Atlas (TCGA) databases and identified an association between Higd-1a levels in colon adenocarcinoma (COAD) tissues and poor survival using Kaplan–Meier curves. Subsequently, we overexpressed Higd-1a in the human COAD cell line HCT-8, knocked down Higd-1a expression in SW480 cells, and evaluated the effects via quantitative PCR (qPCR) and western blotting. MTT assays, colony formation assay, cell cycle analysis, annexin V-FITC/PI, wound-healing analysis, and transwell assay were used to test cell proliferation, formation of cell colonies, cell cycle progression, migration, invasiveness, and apoptosis. Higd-1a has low transcription levels in COAD tissue and suggests a poor prognosis. Higd-1a overexpression in HCT-8 cells weakened cell proliferation, formation of cell colonies, cell cycle progression, migration ability, and invasiveness, and increased apoptosis. Moreover, the decrease of Higd-1a in SW480 cells induced cell proliferation, formation of cell colonies, cell cycle progression, migration, and invasion, and inhibited apoptosis. Higd-1a is underexpressed in COAD cells and its overexpression impaired the proliferation, migration, and invasiveness of COAD cells.
format article
author Zhenyu Xu
Junjie Sun
Yang Chen
Ting Zhang
Yan Qin
Dong Hua
author_facet Zhenyu Xu
Junjie Sun
Yang Chen
Ting Zhang
Yan Qin
Dong Hua
author_sort Zhenyu Xu
title HIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells
title_short HIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells
title_full HIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells
title_fullStr HIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells
title_full_unstemmed HIG1 domain family member 1A disrupts proliferation, migration and invasion of colon adenocarcinoma cells
title_sort hig1 domain family member 1a disrupts proliferation, migration and invasion of colon adenocarcinoma cells
publisher Taylor & Francis Group
publishDate 2021
url https://doaj.org/article/9cd6e79feedd483f957b4573ab889015
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AT junjiesun hig1domainfamilymember1adisruptsproliferationmigrationandinvasionofcolonadenocarcinomacells
AT yangchen hig1domainfamilymember1adisruptsproliferationmigrationandinvasionofcolonadenocarcinomacells
AT tingzhang hig1domainfamilymember1adisruptsproliferationmigrationandinvasionofcolonadenocarcinomacells
AT yanqin hig1domainfamilymember1adisruptsproliferationmigrationandinvasionofcolonadenocarcinomacells
AT donghua hig1domainfamilymember1adisruptsproliferationmigrationandinvasionofcolonadenocarcinomacells
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