Literature DB >> 20920999

Prospective immunohistochemical analysis of primary colorectal cancers for loss of mismatch repair protein expression.

Steven A Lee-Kong1, Arnold J Markowitz, Emily Glogowski, Christopher Papadopoulos, Zsofia Stadler, Martin R Weiser, Larissa K Temple, José G Guillem.   

Abstract

BACKGROUND: Evaluation of patients for Lynch syndrome includes assessment of age and family cancer history as well as testing for microsatellite instability and alterations in mismatch repair (MMR) genes. We examined the value of routine immunohistochemistry (IHC) for MMR proteins in patients with colorectal cancer (CRC) undergoing resection at a single institution. PATIENTS AND METHODS: Beginning in July 2006, all patients aged < 50 years who were undergoing resection of primary CRC had their specimens routinely examined by IHC for MMR proteins. Patients aged 50-60 years were examined if histopathology suggestive of Lynch syndrome was reported, and patients of any age were examined if strong clinical suspicion was present. Family cancer history was analyzed and fulfillment of Amsterdam II criteria determined.
RESULTS: Over an 18-month period, 96 patients aged < 50 years underwent CRC resection. Out of these, 72 patients (75%) had immunohistochemical testing, with an overall MMR protein loss rate of 19%. In selected patients aged 50-60 years and > 60 years, loss rates were 26% and 65%, respectively. Of all patients with MMR protein loss, 10 (32%) had reported histopathology, and 3 (10%) had family histories suggesting Lynch syndrome.
CONCLUSION: We demonstrate the feasibility of routine immunohistochemical testing for MMR proteins in patients with CRC. As only a minority of patients with MMR protein loss met Amsterdam II criteria or had suggestive histopathology reported, routine IHC may identify patients with Lynch syndrome who might otherwise be missed.

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Year:  2010        PMID: 20920999     DOI: 10.3816/CCC.2010.n.038

Source DB:  PubMed          Journal:  Clin Colorectal Cancer        ISSN: 1533-0028            Impact factor:   4.481


  4 in total

1.  Prevalence and clinicopathologic/molecular characteristics of mismatch repair-deficient colorectal cancer in the under-50-year-old Japanese population.

Authors:  Okihide Suzuki; Hidetaka Eguchi; Noriyasu Chika; Takehiko Sakimoto; Keiichiro Ishibashi; Kensuke Kumamoto; Jun-Ichi Tamaru; Tetsuhiko Tachikawa; Kiwamu Akagi; Tomio Arai; Yasushi Okazaki; Hideyuki Ishida
Journal:  Surg Today       Date:  2017-03-03       Impact factor: 2.549

2.  Prevalence and clinicopathological characteristics of mismatch repair-deficient colorectal carcinoma in early onset cases as compared with late-onset cases: a retrospective cross-sectional study in Northeastern Iran.

Authors:  Ladan Goshayeshi; Kamran Ghaffarzadegan; Alireza Khooei; Abbas Esmaeilzadeh; Mahla Rahmani Khorram; Hooman Mosannen Mozaffari; Behzad Kiani; Benyamin Hoseini
Journal:  BMJ Open       Date:  2018-08-30       Impact factor: 2.692

3.  Frequency of Mismatch Repair Protein (MMRP) Deficiency among Young Jordanians Diagnosed with Colorectal Carcinoma (CRC).

Authors:  Bayan Maraqa; Ghassan Al-Shbool; Osama Abu-Shawer; Mamoun Souleiman; Osama Alshakhatreh; Amal Al-Omari; Hadeel Abdelkhaleq; Ayat Taqash; Maysa Al-Hussaini
Journal:  Gastroenterol Res Pract       Date:  2020-04-23       Impact factor: 2.260

4.  Worldwide variation in lynch syndrome screening: case for universal screening in low colorectal cancer prevalence areas.

Authors:  George Kunnackal John; Vipin Das Villgran; Christine Caufield-Noll; Francis Giardiello
Journal:  Fam Cancer       Date:  2020-09-11       Impact factor: 2.375

  4 in total

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