Update on hereditary colorectal cancer

Wernhoff, Patrik (author): Lund University,Lunds universitet,Muskelbiologi,Forskargrupper vid Lunds universitet,Muscle Biology,Lund University Research Groups

(creator_code:org_t)

Anticancer Research USA Inc. 2016
2016
English 8 s.
In: Anticancer research. - : Anticancer Research USA Inc.. - 0250-7005. ; 36:9, s. 4399-4406

Related links:: http://dx.doi.org/10...; show more...; http://ar.iiarjourna...; https://lup.lub.lu.s...; https://doi.org/10.2...; show less...

Abstract Subject headings

In the past two decades, significant advances have been made in our understanding of colorectal (CRC) tumors with DNA mismatch (MMR) repair deficiency. The knowledge from molecular and genetic alterations in a variety of clinical conditions has refined the disease terminology and classification. Hereditary non-polyposis colorectal cancer (HNPCC) encompasses a spectrum of conditions that have significant phenotypic overlapping that makes clinical diagnosis a challenging task. Distinguishing among the HNPCC disorders is clinically important, as the approach to surveillance for patients and their at-risk family members differs according to risks for colonic and extracolonic cancer associated with each syndrome. Prospective and next-generation studies will provide valuable clinical information regarding the natural history of disease that will help differentiate the Lynch syndrome mimics and guide diagnosis and management for heterogeneous conditions currently grouped under the category of familial CRC. The review is intended to present and discuss the molecular nature of various conditions related to MMR deficiency and discusses the tools and strategies that have been used in detecting these conditions.

By the author/editor: Da Silva, Felipe ...; Wernhoff, Patrik; Dominguez-Barrer ...; Dominguez-Valent ...

About the subject

MEDICAL AND HEALTH SCIENCES: MEDICAL AND HEAL ...; and Clinical Medicin ...; and Cancer and Oncol ...

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