Identification and Characterization of the Wilms Tumor Cancer Stem Cell

Author:

Petrosyan Astgik12ORCID,Villani Valentina1,Aguiari Paola13,Thornton Matthew E.4,Wang Yizhou5,Rajewski Alex5,Zhou Shengmei6,Cravedi Paolo7,Grubbs Brendan H.4,De Filippo Roger E.12,Sedrakyan Sargis12,Lemley Kevin V.28,Csete Marie9,Da Sacco Stefano12ORCID,Perin Laura12ORCID

Affiliation:

1. GOFARR Laboratory Children's Hospital Los Angeles Division of Urology Saban Research Institute Los Angeles CA 90027 USA

2. Keck School of Medicine University of Southern California Los Angeles CA 90033 USA

3. David Geffen School of Medicine at UCLA – VA Healthcare System Los Angeles CA 90095 USA

4. Department of Obstetrics and Gynecology Keck School of Medicine University of Southern California Los Angeles CA 90033 USA

5. Genomics Core Department of Biomedical Sciences Cedars‐Sinai Medical Center Los Angeles CA 90048 USA

6. Department of Pathology and Laboratory Medicine Children's Hospital Los Angeles Los Angeles CA 90027 USA

7. Department of Medicine Division of Nephrology and Translational Transplant Research Center Recanati Miller Transplant Institute Icahn School of Medicine at Mount Sinai New York NY 10029 USA

8. Children's Hospital Los Angeles Division of Nephrology Department of Pediatrics University of Southern California Los Angeles CA 90027 USA

9. Department of Anesthesiology University of Southern California Los Angeles CA 90033 USA

Abstract

AbstractA nephrogenic progenitor cell (NP) with cancer stem cell characteristics driving Wilms tumor (WT) using spatial transcriptomics, bulk and single cell RNA sequencing, and complementary in vitro and transplantation experiments is identified and characterized. NP from WT samples with NP from the developing human kidney is compared. Cells expressing SIX2 and CITED1 fulfill cancer stem cell criteria by reliably recapitulating WT in transplantation studies. It is shown that self‐renewal versus differentiation in SIX2+CITED1+ cells is regulated by the interplay between integrins ITGβ1 and ITGβ4. The spatial transcriptomic analysis defines gene expression maps of SIX2+CITED1+ cells in WT samples and identifies the interactive gene networks involved in WT development. These studies define SIX2+CITED1+ cells as the nephrogenic‐like cancer stem cells of WT and points to the renal developmental transcriptome changes as a possible driver in regulating WT formation and progression.

Funder

Pablove Foundation

Publisher

Wiley

Subject

General Physics and Astronomy,General Engineering,Biochemistry, Genetics and Molecular Biology (miscellaneous),General Materials Science,General Chemical Engineering,Medicine (miscellaneous)

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Roles and signaling pathways of CITED1 in tumors: overview and novel insights;Journal of International Medical Research;2024-01

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