IGF2 is Deregulated During the Development of Uterine Cervical Carcinoma in Indian Patients.
Cervical cancer (CACX)
Gene regulation
Insulin-like growth factor 2 (IGF2)
Methylation-specific PCR (MSP)
Normal cervical epithelium (NCE)
Journal
Biochemical genetics
ISSN: 1573-4927
Titre abrégé: Biochem Genet
Pays: United States
ID NLM: 0126611
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
10
11
2018
accepted:
27
03
2019
pubmed:
6
4
2019
medline:
22
11
2019
entrez:
6
4
2019
Statut:
ppublish
Résumé
Uterine cervical carcinoma (CACX) is one of the leading causes of deaths in Indian women. Chromosomal alterations including 11p15.5 locus were reported in CACX. Consequently, we strived for the first time to understand the molecular status of the candidate gene Insulin-like growth factor 2, IGF2 (11p15.5) in Indian CACX patients (n = 128). DNA copy number (CN) analysis using CGH-SNP analysis showed no genetic alteration and it was further validated by comparison with publicly available CN datasets. But promoter hypo-methylation during the progression of CACX was observed and also found to be concordant with publicly available DNA methylation datasets. Interestingly, we found diverse expression of IGF2 transcript in both normal cervical epithelium (NCE) and CACX tumors. Similar heterogeneous expression pattern was seen in publicly available expression datasets as well. Finally, protein expression analysis in NCE showed concordance with transcript expression but tumors showed frequent low expression. Log-rank test showed a difference (p-value = 0.057) in overall survival between cases with and without alteration for IGF2 in Indian CACX patients. Collectively, our study proposes that regulation of IGF2 expression in NCE appeared to be multifaceted and deregulation during the development of CACX resulted in the differential expression.
Identifiants
pubmed: 30949792
doi: 10.1007/s10528-019-09917-1
pii: 10.1007/s10528-019-09917-1
doi:
Substances chimiques
IGF2 protein, human
0
Neoplasm Proteins
0
Insulin-Like Growth Factor II
67763-97-7
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
638-651Subventions
Organisme : University Grants Commission
ID : 2121130723
Organisme : University Grants Commission
ID : 2061430780
Organisme : Council of Scientific and Industrial Research
ID : 60(0111)/14/EMR-II