IGF2 is Deregulated During the Development of Uterine Cervical Carcinoma in Indian Patients.


Journal

Biochemical genetics
ISSN: 1573-4927
Titre abrégé: Biochem Genet
Pays: United States
ID NLM: 0126611

Informations de publication

Date de publication:
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

638-651

Subventions

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

Auteurs

Anirban Roychowdhury (A)

Department of Oncogene Regulation, Chittaranjan National Cancer Institute, 37, S. P. Mukherjee Road, Kolkata, 700 026, India.

Sudip Samadder (S)

Department of Oncogene Regulation, Chittaranjan National Cancer Institute, 37, S. P. Mukherjee Road, Kolkata, 700 026, India.

Dipanjana Indra Mazumder (D)

Department of Zoology, Siliguri College, Darjeeling, India.

Pijush Das (P)

Structural Biology and Bioinformatics Division, CSIR-Indian Institute of Chemical Biology, Kolkata, India.

Mukta Basu (M)

Department of Oncogene Regulation, Chittaranjan National Cancer Institute, 37, S. P. Mukherjee Road, Kolkata, 700 026, India.

Ranajit Mondal (R)

Department of Gynecology Oncology, Chittaranjan National Cancer Institute, Kolkata, India.

Anup Roy (A)

Department of Pathology, Nil Ratan Sircar Medical College and Hospital, Kolkata, India.

Susanta Roychoudhury (S)

Saroj Gupta Cancer Centre & Research Institute, Kolkata, India.

Chinmay Kumar Panda (CK)

Department of Oncogene Regulation, Chittaranjan National Cancer Institute, 37, S. P. Mukherjee Road, Kolkata, 700 026, India. ckpanda.cnci@gmail.com.

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Classifications MeSH