» Articles » PMID: 9809551

Loss of Imprinting in Normal Tissue of Colorectal Cancer Patients with Microsatellite Instability

Overview
Journal Nat Med
Date 1998 Nov 11
PMID 9809551
Citations 75
Authors
Affiliations
Soon will be listed here.
Abstract

Loss of imprinting (LOI) is an epigenetic alteration of some cancers involving loss of parental origin-specific expression of imprinted genes. We observed LOI of the insulin-like growth factor-II gene in twelve of twenty-seven informative colorectal cancer patients (44%), as well as in the matched normal colonic mucosa of the patients with LOI in their cancers, and in peripheral blood samples of four patients. Ten of eleven cancers (91%) with microsatellite instability showed LOI, compared with only two of sixteen tumors (12%) without microsatellite instability (P < 0.001). Control patients without cancer showed LOI in colonic mucosa of only two of sixteen cases (12%, P < 0.001) and two of fifteen blood samples (13%, P < 0.001). These data suggest that LOI in tumor and normal tissue identifies most colorectal cancer patients with microsatellite instability in their tumors, and that LO! may identify an important subset of the population with cancer or at risk of developing cancer.

Citing Articles

Altered methylation of imprinted genes in neuroblastoma: implications for prognostic refinement.

Suman M, Lofgren M, Fransson S, Yousuf J, Svensson J, Djos A J Transl Med. 2024; 22(1):808.

PMID: 39217334 PMC: 11366169. DOI: 10.1186/s12967-024-05634-5.


The role of imprinting genes' loss of imprints in cancers and their clinical implications.

Xie G, Si Q, Zhang G, Fan Y, Li Q, Leng P Front Oncol. 2024; 14:1365474.

PMID: 38812777 PMC: 11133587. DOI: 10.3389/fonc.2024.1365474.


Molecular and genetic targets within metastatic colorectal cancer and associated novel treatment advancements.

Cann C, LaPelusa M, Cimino S, Eng C Front Oncol. 2023; 13:1176950.

PMID: 37409250 PMC: 10319053. DOI: 10.3389/fonc.2023.1176950.


Insulin-like growth factor 2 (IGF2) expression in adrenocortical disease due to PRKAR1A mutations compared to other benign adrenal tumors.

Nadella K, Berthon A, Almeida M, Levy I, Faucz F, Stratakis C Endocrine. 2021; 72(3):823-834.

PMID: 33420948 DOI: 10.1007/s12020-020-02583-z.


Hypermethylation of the non-imprinted maternal MEG3 and paternal MEST alleles is highly variable among normal individuals.

Haertle L, Maierhofer A, Bock J, Lehnen H, Bottcher Y, Bluher M PLoS One. 2017; 12(8):e0184030.

PMID: 28854270 PMC: 5576652. DOI: 10.1371/journal.pone.0184030.