Details

Autor(en) / Beteiligte

• Suerink, Manon
• van der Klift, Heleen M.
• ten Broeke, Sanne W.
• Dekkers, Olaf M.
• Bernstein, Inge
• Capellá Munar, Gabriel
• Gomez Garcia, Encarna
• Hoogerbrugge, Nicoline
• Letteboer, Tom G.W.
• Menko, Fred H.
• Lindblom, Annika
• Mensenkamp, Arjen
• Moller, Pal
• van Os, Theo A.
• Rahner, Nils
• Redeker, Bert J.W.
• Olderode, Maran
• Spruijt, Liesbeth
• Vos, Yvonne J.
• Wagner, Anja
• Morreau, Hans
• Hes, Frederik J.
• Vasen, Hans F.A.
• Tops, Carli M.
• Wijnen, Juul T.
• Nielsen, Maartje

Titel

The effect of genotypes and parent of origin on cancer risk and age of cancer development in PMS2 mutation carriers

Ist Teil von

• Genetics in medicine, 2016-04, Vol.18 (4), p.405-409

Ort / Verlag

United States: Elsevier Inc

Erscheinungsjahr

2016

Quelle

MEDLINE

Beschreibungen/Notizen

• Lynch syndrome (LS), a heritable disorder with an increased risk of primarily colorectal cancer (CRC) and endometrial cancer (EC), can be caused by mutations in the PMS2 gene. We wished to establish whether genotype and/or parent-of-origin effects (POE) explain (part of) the reported variability in severity of the phenotype. European PMS2 mutation carriers (n = 381) were grouped and compared based on RNA expression and whether the mutation was inherited paternally or maternally. Mutation carriers with loss of RNA expression (group 1) had a significantly lower age at CRC diagnosis (51.1 years vs. 60.0 years, P = 0.035) and a lower age at EC diagnosis (55.8 years vs. 61.0 years, P = 0.2, nonsignificant) compared with group 2 (retention of RNA expression). Furthermore, group 1 showed slightly higher, but nonsignificant, hazard ratios (HRs) for both CRC (HR: 1.31, P = 0.38) and EC (HR: 1.22, P = 0.72). No evidence for a significant parent-of-origin effect was found for either CRC or EC. PMS2 mutation carriers with retention of RNA expression developed CRC 9 years later than those with loss of RNA expression. If confirmed, this finding would justify a delay in surveillance for these cases. Cancer risk was not influenced by a parent-of-origin effect.