Deficient DNA mismatch repair is associated with favorable prognosis in Thai patients with sporadic colorectal cancer

doi:10.3748/wjg.v21.i3.926

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World Journal of Gastroenterology

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1007-9327

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Baishideng Publishing Group Inc, 7041 Koll Center Parkway, Suite 160, Pleasanton, CA 94566, USA

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World J Gastroenterol. Jan 21, 2015; 21(3): 926-934
Published online Jan 21, 2015. doi: 10.3748/wjg.v21.i3.926

Table 3 Prevalence of mismatch repair and BRAF status n (%)

Variables	All cases
MMR status	n = 211
IHC method	164 (77.73)
pMMR	154
dMMR	10
MLH-1	4
MSH-2	6
MSH-6	0
PMS-2	0
MSI method	44 (20.85)
MSI-H	21
MSI-L/MSI-S	23
Unknown	3 (1.42)
BRAF status
Wild type	188 (89.1)
Mutation	23 (10.9)

pMMR: Proficient mismatch repair; dMMR: Deficient mismatch repair; MSI-H: High-level MSI; MSI-L: Low-level MSI; MSS: Microsatellite stable.

Citation: Korphaisarn K, Pongpaibul A, Limwongse C, Roothumnong E, Klaisuban W, Nimmannit A, Jinawath A, Akewanlop C. Deficient DNA mismatch repair is associated with favorable prognosis in Thai patients with sporadic colorectal cancer. World J Gastroenterol 2015; 21(3): 926-934
URL: https://www.wjgnet.com/1007-9327/full/v21/i3/926.htm
DOI: https://dx.doi.org/10.3748/wjg.v21.i3.926