TY - JOUR
T1 - PMS2-associated Lynch syndrome
T2 - Past, present and future
AU - Andini, Katarina D.
AU - Nielsen, Maartje
AU - Suerink, Manon
AU - Helderman, Noah C.
AU - Koornstra, Jan Jacob
AU - Ahadova, Aysel
AU - Kloor, Matthias
AU - Mourits, Marian J.E.
AU - Kok, Klaas
AU - Sijmons, Rolf H.
AU - Bajwa–ten Broeke, Sanne W.
N1 - Funding Information:
KA and SB are being funded by the Dutch Cancer Society. Grant number: KWF 2019-2/12570. Acknowledgments
Publisher Copyright:
Copyright © 2023 Andini, Nielsen, Suerink, Helderman, Koornstra, Ahadova, Kloor, Mourits, Kok, Sijmons and Bajwa–ten Broeke.
PY - 2023/2/21
Y1 - 2023/2/21
N2 - Carriers of any pathogenic variant in one of the MMR genes (path_MMR carriers) were traditionally thought to be at comparable risk of developing a range of different malignancies, foremost colorectal cancer (CRC) and endometrial cancer. However, it is now widely accepted that their cancer risk and cancer spectrum range notably depending on which MMR gene is affected. Moreover, there is increasing evidence that the MMR gene affected also influences the molecular pathogenesis of Lynch syndrome CRC. Although substantial progress has been made over the past decade in understanding these differences, many questions remain unanswered, especially pertaining to path_PMS2 carriers. Recent findings show that, while the cancer risk is relatively low, PMS2-deficient CRCs tend to show more aggressive behaviour and have a worse prognosis than other MMR-deficient CRCs. This, together with lower intratumoral immune infiltration, suggests that PMS2-deficient CRCs might have more in common biologically with sporadic MMR-proficient CRCs than with other MMR-deficient CRCs. These findings could have important consequences for surveillance, chemoprevention and therapeutic strategies (e.g. vaccines). In this review we discuss the current knowledge, current (clinical) challenges and knowledge gaps that should be targeted by future studies.
AB - Carriers of any pathogenic variant in one of the MMR genes (path_MMR carriers) were traditionally thought to be at comparable risk of developing a range of different malignancies, foremost colorectal cancer (CRC) and endometrial cancer. However, it is now widely accepted that their cancer risk and cancer spectrum range notably depending on which MMR gene is affected. Moreover, there is increasing evidence that the MMR gene affected also influences the molecular pathogenesis of Lynch syndrome CRC. Although substantial progress has been made over the past decade in understanding these differences, many questions remain unanswered, especially pertaining to path_PMS2 carriers. Recent findings show that, while the cancer risk is relatively low, PMS2-deficient CRCs tend to show more aggressive behaviour and have a worse prognosis than other MMR-deficient CRCs. This, together with lower intratumoral immune infiltration, suggests that PMS2-deficient CRCs might have more in common biologically with sporadic MMR-proficient CRCs than with other MMR-deficient CRCs. These findings could have important consequences for surveillance, chemoprevention and therapeutic strategies (e.g. vaccines). In this review we discuss the current knowledge, current (clinical) challenges and knowledge gaps that should be targeted by future studies.
KW - carcinonogenesis
KW - colorectal cancer
KW - endometrial cancer
KW - Lynch syndrome (hereditary nonpolyposis colorectal cancer)
KW - mismatch repair (MMR)
KW - PMS2 gene
U2 - 10.3389/fonc.2023.1127329
DO - 10.3389/fonc.2023.1127329
M3 - Review article
C2 - 36895471
AN - SCOPUS:85149675138
SN - 2234-943X
VL - 13
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 1127329
ER -