TY - JOUR
T1 - Mex3a marks drug-tolerant persister colorectal cancer cells that mediate relapse after chemotherapy
AU - Álvarez-Varela, Adrián
AU - Novellasdemunt, Laura
AU - Barriga, Francisco M.
AU - Hernando-Momblona, Xavier
AU - Cañellas-Socias, Adrià
AU - Cano-Crespo, Sara
AU - Sevillano, Marta
AU - Cortina, Carme
AU - Stork, Diana
AU - Morral, Clara
AU - Turon, Gemma
AU - Slebe, Felipe
AU - Jiménez-Gracia, Laura
AU - Caratù, Ginevra
AU - Jung, Peter
AU - Stassi, Giorgio
AU - Heyn, Holger
AU - Tauriello, Daniele V.F.
AU - Mateo, Lidia
AU - Tejpar, Sabine
AU - Sancho, Elena
AU - Stephan-Otto Attolini, Camille
AU - Batlle, Eduard
N1 - Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature America, Inc.
PY - 2022/9
Y1 - 2022/9
N2 - Colorectal cancer (CRC) patient-derived organoids predict responses to chemotherapy. Here we used them to investigate relapse after treatment. Patient-derived organoids expand from highly proliferative LGR5+ tumor cells; however, we discovered that lack of optimal growth conditions specifies a latent LGR5+ cell state. This cell population expressed the gene MEX3A, is chemoresistant and regenerated the organoid culture after treatment. In CRC mouse models, Mex3a+ cells contributed marginally to metastatic outgrowth; however, after chemotherapy, Mex3a+ cells produced large cell clones that regenerated the disease. Lineage-tracing analysis showed that persister Mex3a+ cells downregulate the WNT/stem cell gene program immediately after chemotherapy and adopt a transient state reminiscent to that of YAP+ fetal intestinal progenitors. In contrast, Mex3a-deficient cells differentiated toward a goblet cell-like phenotype and were unable to resist chemotherapy. Our findings reveal that adaptation of cancer stem cells to suboptimal niche environments protects them from chemotherapy and identify a candidate cell of origin of relapse after treatment in CRC.
AB - Colorectal cancer (CRC) patient-derived organoids predict responses to chemotherapy. Here we used them to investigate relapse after treatment. Patient-derived organoids expand from highly proliferative LGR5+ tumor cells; however, we discovered that lack of optimal growth conditions specifies a latent LGR5+ cell state. This cell population expressed the gene MEX3A, is chemoresistant and regenerated the organoid culture after treatment. In CRC mouse models, Mex3a+ cells contributed marginally to metastatic outgrowth; however, after chemotherapy, Mex3a+ cells produced large cell clones that regenerated the disease. Lineage-tracing analysis showed that persister Mex3a+ cells downregulate the WNT/stem cell gene program immediately after chemotherapy and adopt a transient state reminiscent to that of YAP+ fetal intestinal progenitors. In contrast, Mex3a-deficient cells differentiated toward a goblet cell-like phenotype and were unable to resist chemotherapy. Our findings reveal that adaptation of cancer stem cells to suboptimal niche environments protects them from chemotherapy and identify a candidate cell of origin of relapse after treatment in CRC.
UR - http://www.scopus.com/inward/record.url?scp=85133206443&partnerID=8YFLogxK
UR - https://diposit.ub.edu/dspace/bitstream/2445/191038/1/NatCan_Alvarez-Varela_2022.pdf
U2 - 10.1038/s43018-022-00402-0
DO - 10.1038/s43018-022-00402-0
M3 - Article
C2 - 35773527
AN - SCOPUS:85133206443
SN - 2662-1347
VL - 3
SP - 1052
EP - 1070
JO - Nature Cancer
JF - Nature Cancer
IS - 9
ER -