TY - JOUR
T1 - Is HLA type a possible cancer risk modifier in Lynch syndrome?
AU - Ahadova, Aysel
AU - Witt, Johannes
AU - Haupt, Saskia
AU - Gallon, Richard
AU - Hüneburg, Robert
AU - Nattermann, Jacob
AU - ten Broeke, Sanne
AU - Bohaumilitzky, Lena
AU - Hernandez-Sanchez, Alejandro
AU - Santibanez-Koref, Mauro
AU - Jackson, Michael S.
AU - Ahtiainen, Maarit
AU - Pylvänäinen, Kirsi
AU - Andini, Katarina
AU - Grolmusz, Vince Kornel
AU - Möslein, Gabriela
AU - Dominguez-Valentin, Mev
AU - Møller, Pål
AU - Fürst, Daniel
AU - Sijmons, Rolf
AU - Borthwick, Gillian M.
AU - Burn, John
AU - Mecklin, Jukka Pekka
AU - Heuveline, Vincent
AU - von Knebel Doeberitz, Magnus
AU - Seppälä, Toni
AU - Kloor, Matthias
N1 - Funding Information:
AsCaP collaboration; Cancer Research UK Catalyst Award, Grant/Award Number: C569/A24991; CAPP3 Clinical Research Committee Late Phase Award, Grant/Award Number: A15934; Deutsche Forschungsgemeinschaft; Deutsche Krebshilfe, Grant/Award Number: 70113455; Donations against Cancer, NCT Heidelberg; Else‐Kröner‐Fresenius Foundation, Grant/Award Number: 2018_A44; Emil Aaltosen Säätiö; Finnish Cancer Society; Jane ja Aatos Erkon Säätiö; National Research, Development and Innovation Office, Hungary, Grant/Award Number: NKFIH‐FK‐21‐138377; Suomen Lääketieteen Säätiö; Wilhelm Sander Foundation; Klaus Tschira Foundation, Grant/Award Number: 00.012.2021 Funding information
Funding Information:
Previous studies leading to the constitution of the hypothesis have been supported by Wilhelm Sander Foundation, Deutsche Krebshilfe (German Cancer Aid, 70113455), German Research Foundation, “Donations against Cancer” program of the NCT Heidelberg. Pilot experiments were supported by the Else‐Kröner‐Fresenius Foundation, AsCaP collaboration and Cancer research UK Catalyst Award (Grant Number: C569/A24991), the CaPP3 Clinical Research Committee Late Phase Award (A15934), Finnish Medical Foundation, Emil Aaltonen Foundation, Finnish Cancer Society, Jane and Aatos Erkko foundation and the National Research, Development and Innovation Office (Hungary, NKFIH‐FK‐21‐138377). Mathematical analyses were supported by the Klaus Tschira Foundation, Heidelberg, Germany in frame of the project “Mathematics in Oncology—Towards optimal prevention and treatment in patients with inherited cancer syndrome.”
Publisher Copyright:
© 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
PY - 2023
Y1 - 2023
N2 - Lynch syndrome (LS) is the most common inherited cancer syndrome. It is inherited via a monoallelic germline variant in one of the DNA mismatch repair (MMR) genes. LS carriers have a broad 30% to 80% risk of developing various malignancies, and more precise, individual risk estimations would be of high clinical value, allowing tailored cancer prevention and surveillance. Due to MMR deficiency, LS cancers are characterized by the accumulation of frameshift mutations leading to highly immunogenic frameshift peptides (FSPs). Thus, immune surveillance is proposed to inhibit the outgrowth of MMR-deficient cell clones. Recent studies have shown that immunoediting during the evolution of MMR-deficient cancers leads to a counter-selection of highly immunogenic antigens. The immunogenicity of FSPs is dependent on the antigen presentation. One crucial factor determining antigen presentation is the HLA genotype. Hence, a LS carrier's HLA genotype plays an important role in the presentation of FSP antigens to the immune system, and may influence the likelihood of progression from precancerous lesions to cancer. To address the challenge of clarifying this possibility including diverse populations with different HLA types, we have established the INDICATE initiative (Individual cancer risk by HLA type, http://indicate-lynch.org/), an international network aiming at a systematic evaluation of the HLA genotype as a possible cancer risk modifier in LS. Here we summarize the current knowledge on the role of HLA type in cancer risk and outline future research directions to delineate possible association in the scenario of LS with genetically defined risk population and highly immunogenic tumors.
AB - Lynch syndrome (LS) is the most common inherited cancer syndrome. It is inherited via a monoallelic germline variant in one of the DNA mismatch repair (MMR) genes. LS carriers have a broad 30% to 80% risk of developing various malignancies, and more precise, individual risk estimations would be of high clinical value, allowing tailored cancer prevention and surveillance. Due to MMR deficiency, LS cancers are characterized by the accumulation of frameshift mutations leading to highly immunogenic frameshift peptides (FSPs). Thus, immune surveillance is proposed to inhibit the outgrowth of MMR-deficient cell clones. Recent studies have shown that immunoediting during the evolution of MMR-deficient cancers leads to a counter-selection of highly immunogenic antigens. The immunogenicity of FSPs is dependent on the antigen presentation. One crucial factor determining antigen presentation is the HLA genotype. Hence, a LS carrier's HLA genotype plays an important role in the presentation of FSP antigens to the immune system, and may influence the likelihood of progression from precancerous lesions to cancer. To address the challenge of clarifying this possibility including diverse populations with different HLA types, we have established the INDICATE initiative (Individual cancer risk by HLA type, http://indicate-lynch.org/), an international network aiming at a systematic evaluation of the HLA genotype as a possible cancer risk modifier in LS. Here we summarize the current knowledge on the role of HLA type in cancer risk and outline future research directions to delineate possible association in the scenario of LS with genetically defined risk population and highly immunogenic tumors.
KW - cancer immunoediting
KW - HLA genotype
KW - immune surveillance
KW - Lynch syndrome
KW - personalized cancer risk
U2 - 10.1002/ijc.34312
DO - 10.1002/ijc.34312
M3 - Review Article
C2 - 36214792
AN - SCOPUS:85139914047
SN - 0020-7136
VL - 152
SP - 2024
EP - 2031
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 10
ER -