Literature DB >> 19723644

Molecular analysis of endometrial tumorigenesis: importance of complex hyperplasia regardless of atypia.

Taina T Nieminen1, Annette Gylling, Wael M Abdel-Rahman, Kyösti Nuorva, Markku Aarnio, Laura Renkonen-Sinisalo, Heikki J Järvinen, Jukka-Pekka Mecklin, Ralf Bützow, Päivi Peltomäki.   

Abstract

PURPOSE: Endometrial carcinoma (EC) is common in the population and the most frequent extracolonic malignancy in hereditary nonpolyposis colorectal carcinoma (HNPCC)/Lynch syndrome. We characterized precursor lesions of endometrioid EC to identify markers of malignant transformation and tumor progression. EXPERIMENTAL
DESIGN: Serial specimens of normal endometrium, simple hyperplasia, complex hyperplasia without atypia, complex hyperplasia with atypia, and endometrial carcinoma obtained during a 10-year surveillance of DNA mismatch repair (MMR) gene mutation carriers (together 110 samples) were molecularly profiled and compared with a sporadic reference series of endometrial specimens taken for nonmalignant reasons (62 samples).
RESULTS: Among MMR gene mutation carriers, decreased MMR protein expression was present in 7% in normal endometrium, 40% in simple hyperplasia, 100% in complex hyperplasia without atypia, 92% in complex hyperplasia with atypia, and 100% in endometrial carcinoma. Microsatellite instability frequencies were lower (6%, 17%, 67%, 38%, and 64%, respectively). Among 24 tumor suppressor genes, the number of methylated loci increased from normal endometrium to simple hyperplasia to complex hyperplasia (complex hyperplasia without atypia/complex hyperplasia with atypia) in both Lynch syndrome and reference series. The most frequently methylated genes were CDH13, RASSF1A, and GSTP1. In MMR gene mutation carriers, MMR and methylation defects appeared up to 12 years before endometrial carcinoma.
CONCLUSIONS: Molecular changes in endometrial tissue are detectable several years before endometrial carcinoma in genetically predisposed individuals. Abnormal MMR and methylation classify normal endometrium and simple hyperplasia into one category and complex hyperplasia without atypia, complex hyperplasia with atypia, and endometrial carcinoma into another, suggesting that, contrary to a traditional view, complex hyperplasia without atypia and complex hyperplasia with atypia are equally important as precursor lesions of endometrial carcinoma.

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Year:  2009        PMID: 19723644     DOI: 10.1158/1078-0432.CCR-09-0506

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  23 in total

1.  Body mass index in early adulthood and endometrial cancer risk for mismatch repair gene mutation carriers.

Authors:  Aung Ko Win; James G Dowty; Yoland C Antill; Dallas R English; John A Baron; Joanne P Young; Graham G Giles; Melissa C Southey; Ingrid Winship; Lara Lipton; Susan Parry; Stephen N Thibodeau; Robert W Haile; Steven Gallinger; Loïc Le Marchand; Noralane M Lindor; Polly A Newcomb; John L Hopper; Mark A Jenkins
Journal:  Obstet Gynecol       Date:  2011-04       Impact factor: 7.661

2.  Mismatch repair system in endometriotic tissue and eutopic endometrium of unaffected women.

Authors:  Tiziana Grassi; Angelo Calcagno; Stefania Marzinotto; Ambrogio P Londero; Maria Orsaria; Gioia N Canciani; Carlo Alberto Beltrami; Diego Marchesoni; Laura Mariuzzi
Journal:  Int J Clin Exp Pathol       Date:  2015-02-01

3.  Combined colonoscopy and endometrial biopsy cancer screening results in women with Lynch syndrome.

Authors:  Denise R Nebgen; Karen H Lu; Sue Rimes; Elizabeth Keeler; Russell Broaddus; Mark F Munsell; Patrick M Lynch
Journal:  Gynecol Oncol       Date:  2014-08-19       Impact factor: 5.482

4.  Frequent SOCS3 and 3OST2 promoter methylation and their epigenetic regulation in endometrial carcinoma.

Authors:  Haiyan Chen; Cuijuan Zhang; Yan Sheng; Shuzhe Yao; Zhiyan Liu; Cheng Zhang; Tingguo Zhang
Journal:  Am J Cancer Res       Date:  2014-12-15       Impact factor: 6.166

5.  Frequent loss of mutation-specific mismatch repair protein expression in nonneoplastic endometrium of Lynch syndrome patients.

Authors:  Serena Wong; Pei Hui; Natalia Buza
Journal:  Mod Pathol       Date:  2020-01-13       Impact factor: 7.842

Review 6.  DNA methylation in endometrial cancer.

Authors:  Meng Hua Tao; Jo L Freudenheim
Journal:  Epigenetics       Date:  2010-08-16       Impact factor: 4.528

7.  Comparison of lifestyle, hormonal and medical factors in women with sporadic and Lynch syndrome-associated endometrial cancer: A retrospective case-case study.

Authors:  Mari H Aaltonen; Synnöve Staff; Jukka-Pekka Mecklin; Kirsi Pylvänäinen; Johanna U Mäenpää
Journal:  Mol Clin Oncol       Date:  2017-04-06

8.  Causes of death of mutation carriers in Finnish Lynch syndrome families.

Authors:  Kirsi Pylvänäinen; Tuula Lehtinen; Ilmo Kellokumpu; Heikki Järvinen; Jukka-Pekka Mecklin
Journal:  Fam Cancer       Date:  2012-09       Impact factor: 2.375

9.  Molecular profiling of endometrial malignancies.

Authors:  Norasate Samarnthai; Kevin Hall; I-Tien Yeh
Journal:  Obstet Gynecol Int       Date:  2010-03-28

10.  The genomics and genetics of endometrial cancer.

Authors:  Andrea J O'Hara; Daphne W Bell
Journal:  Adv Genomics Genet       Date:  2012-03
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