Although PMS2 mutations or mutations in both PMS2 and p53 are not frequently found in human cancers and thus may be of minor clinical importance, our study may nevertheless contribute to fostering the concept that tumour-targeted functional inhibition of PMS2 may be an adjunct to chemotherapy in the treatment of tumours unresponsive to therapeutic regimens due to mutations in the p53 gene. Here, TP53 is linked to neoplasm.