Utility of p16 immunohistochemistry for the identification of Lynch syndrome

Artemio Payá, Cristina Alenda, Lucía Pérez-Carbonell, Estefanía Rojas, José Luis Soto, Carmen Guillén, Adela Castillejo, Victor M. Barberá, Alfredo Carrato, Antoni Castells, Xavier Llor, Montserrat Andreu, Jim Koh, Greg H. Enders, Susana Benlloch, Rodrigo Jover

Research output: Contribution to journalArticlepeer-review

18 Scopus citations


Purpose: Immunohistochemistry for mismatch repair proteins has shown utility in the identification of Lynch syndrome, but majority of tumors with loss of MLH1expression are due to sporadic hypermethylation of the MLH1 promoter. These tumors can also show epigenetic silencing of other genes, such as p16. The aim of our study is to evaluate the utility of p16 immunohistochemistry in the prediction of MLH1germline mutations. Experimental Design: p16 immunohistochemistry was appropriately evaluated in 79 colorectal cancers with loss of MLH1 expression. Methylation of MLH1 and p16 were quantitatively studied using real-time PCR assay Methylight. BRAF V600E mutation in tumor tissue was also investigated. Genetic testing for germline mutation of MLH1 was made on 52 patients. Results: Loss of p16 expression was seen in 21 of 79 samples (26.6%). There was found statistically significant association between p16 expression and p16 methylation (P < 0.001), MLH1 methylation (P < 0.001), and BRAF mutation (P < 0.005). All tumors with loss of p16 expression showed hypermethylation of p16 (21 of 21), 95.2% (20 of 21) showed MLH1 methylation, and 71.4% (15 of 21) were mutated for BRAF V600E. Mutational analysis showed pathogenic germline mutations in 8 of the patients, harboring 10 tumors. All 10 of these tumors showed normal staining of p16 in the immunochemical analysis. Conclusions: p16 immunohistochemistry is a good surrogate marker for p16 and MLH1 epigenetic silencing due to hypermethylation, and is useful as screening tool in the selection of patients for genetic testing in Lynch syndrome.

Original languageEnglish
Pages (from-to)3156-3162
Number of pages7
JournalClinical Cancer Research
Issue number9
StatePublished - 1 May 2009
Externally publishedYes


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