TY - JOUR
T1 - Diffuse gastric cancer
T2 - Emerging mechanisms of tumor initiation and progression
AU - Monster, Jooske L
AU - Kemp, Lars J S
AU - Gloerich, Martijn
AU - van der Post, Rachel S
N1 - Publisher Copyright:
© 2022 The Authors
PY - 2022/5
Y1 - 2022/5
N2 - Gastric cancer is globally the fourth leading cause of cancer-related deaths. Patients with diffuse-type gastric cancer (DGC) particularly have a poor prognosis that only marginally improved over the last decades, as conventional chemotherapies are frequently ineffective and specific therapies are unavailable. Early-stage DGC is characterized by intramucosal lesions of discohesive cells, which can be present for many years before the emergence of advanced DGC consisting of highly proliferative and invasive cells. The mechanisms underlying the key steps of DGC development and transition to aggressive tumors are starting to emerge. Novel mouse and organoid models for DGC, together with multi-omic analyses of DGC tumors, revealed contributions of both tumor cell-intrinsic alterations and gradual changes in the tumor microenvironment to DGC progression. In this review, we will discuss how these recent findings are leading towards an understanding of the cellular and molecular mechanisms responsible for DGC initiation and malignancy, which may provide opportunities for targeted therapies.
AB - Gastric cancer is globally the fourth leading cause of cancer-related deaths. Patients with diffuse-type gastric cancer (DGC) particularly have a poor prognosis that only marginally improved over the last decades, as conventional chemotherapies are frequently ineffective and specific therapies are unavailable. Early-stage DGC is characterized by intramucosal lesions of discohesive cells, which can be present for many years before the emergence of advanced DGC consisting of highly proliferative and invasive cells. The mechanisms underlying the key steps of DGC development and transition to aggressive tumors are starting to emerge. Novel mouse and organoid models for DGC, together with multi-omic analyses of DGC tumors, revealed contributions of both tumor cell-intrinsic alterations and gradual changes in the tumor microenvironment to DGC progression. In this review, we will discuss how these recent findings are leading towards an understanding of the cellular and molecular mechanisms responsible for DGC initiation and malignancy, which may provide opportunities for targeted therapies.
KW - Animals
KW - Cell Transformation, Neoplastic
KW - Humans
KW - Mice
KW - Stomach Neoplasms/pathology
KW - Tumor Microenvironment
UR - http://www.scopus.com/inward/record.url?scp=85126987985&partnerID=8YFLogxK
U2 - 10.1016/j.bbcan.2022.188719
DO - 10.1016/j.bbcan.2022.188719
M3 - Review article
C2 - 35307354
SN - 0304-419X
VL - 1877
JO - Biochimica et Biophysica Acta-Reviews on Cancer
JF - Biochimica et Biophysica Acta-Reviews on Cancer
IS - 3
M1 - 188719
ER -