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Ovarian tumor cells gain competitive advantage by actively reducing the cellular fitness of microenvironment cells

  • Esha Madan
  • , António M. Palma
  • , Vignesh Vudatha
  • , Amit Kumar
  • , Praveen Bhoopathi
  • , Jochen Wilhelm
  • , Tytus Bernas
  • , Patrick C. Martin
  • , Gaurav Bilolikar
  • , Aenya Gogna
  • , Maria Leonor Peixoto
  • , Isabelle Dreier
  • , Thais Fenz Araujo
  • , Elena Garre
  • , Anna Gustafsson
  • , Kalpana Deepa Priya Dorayappan
  • , Narsimha Mamidi
  • , Zhaoyu Sun
  • , Michail Yekelchyk
  • , Davide Accardi
  • Amalie Lykke Olsen, Lin Lin, Asaf Ashkenazy Titelman, Michael Bianchi, Phil Jessmon, Elnaz Abbasi Farid, Anjan K. Pradhan, Lena Neufeld, Eilam Yeini, Santanu Maji, Christopher J. Pelham, Hyobin Kim, Daniel Oh, Hans Olav Rolfsnes, Rita C. Marques, Amy Lu, Masaki Nagane, Sahil Chaudhary, Kartik Gupta, Keshav C. Gogna, Ana Bigio, Karthikeya Bhoopathi, Padmanabhan Mannangatti, K. Gopinath Achary, Javed Akhtar, Sara Belião, Swadesh Das, Isabel Correia, Cláudia L. da Silva, Arsénio M. Fialho, Michael J. Poellmann, Kaila Javius-Jones, Adam M. Hawkridge, Sanya Pal, Kumari S. Shree, Emad A. Rakha, Sambhav Khurana, Gaoping Xiao, Dongyu Zhang, Arjun Rijal, Charles Lyons, Steven R. Grossman, David P. Turner, Raghavendra Pillappa, Karanvir Prakash, Gaurav Gupta, Gary L.W.G. Robinson, Jennifer Koblinski, Hongjun Wang, Gita Singh, Sujay Singh, Sagar Rayamajhi, Manny D. Bacolod, Hope Richards, Sadia Sayeed, Katherine P. Klein, David Chelmow, Ronit Satchi-Fainaro, Karuppaiyah Selvendiran, Denise Connolly, Frits Alan Thorsen, Rolf Bjerkvig, Kenneth P. Nephew, Michael O. Idowu, Mark P. Kühnel, Christopher Moskaluk, Seungpyo Hong, William L. Redmond, Göran Landberg, Antonio Lopez-Beltran, Andrew S. Poklepovic, Arun Sanyal, Paul B. Fisher, George M. Church, Usha Menon, Ronny Drapkin, Andrew K. Godwin, Yonglun Luo, Maximilian Ackermann, Alexandar Tzankov, Kirsten D. Mertz, Danny Jonigk, Allan Tsung, David Sidransky, Jose Trevino, Arturo P. Saavedra, Robert Winn, Kyoung Jae Won, Eduardo Moreno, Rajan Gogna
  • Virginia Commonwealth University
  • University of Lisbon
  • Justus Liebig University Giessen
  • Cedars-Sinai Medical Center
  • Collegiate School
  • Champalimaud Foundation
  • University of Gothenburg
  • Ohio State University
  • University of Wisconsin-Madison
  • Earle A. Chiles Research Institute
  • Aarhus University
  • Harvard University
  • Empire Genomics Corp.
  • Indiana University Bloomington
  • Tel Aviv University
  • Eurofins GSC Lux SARL
  • University of Bergen
  • Azabu University
  • Imgenex India Pvt. Ltd.
  • INNOMICS INC.
  • Nottingham City Hospital
  • University of Nottingham
  • University of Southern California
  • PhaseDesign Research
  • Stevens Institute of Technology
  • University of Kansas
  • Cornell University
  • Luxembourg Institute of Health
  • Shandong University
  • RWTH Aachen University
  • Hannover Medical School
  • University of Virginia
  • University of Córdoba
  • Centro Clínico Champalimaud
  • University College London
  • University of Pennsylvania
  • Johannes Gutenberg University Mainz
  • Fresenius AG
  • University of Basel
  • Johns Hopkins University

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

Abstract

Cell competition and fitness comparison between cancer and tumor microenvironment (TME) cells determine oncogenic fate. Our previous study established a role for human Flower isoforms as fitness fingerprints, where the expression of Flower Win isoforms in tumor cells leads to growth advantage over TME cells expressing Lose isoforms. Here we demonstrate that the expression of Flower Lose and reduced microenvironment fitness is not a pre-existing condition but, rather, a cancer-induced phenomenon. Cancer cells actively reduce TME fitness by the exosome-mediated release of a cancer-specific long non-coding RNA, Tu-Stroma, which controls the splicing of the Flower gene in the TME cells and expression of Flower Lose isoform, which leads to reduced fitness status. This mechanism controls cancer growth, metastasis and host survival in ovarian cancer. Targeting Flower protein with humanized monoclonal antibody (mAb) in mice significantly reduces cancer growth and metastasis and improves survival. Pre-treatment with Flower mAb protects intraperitoneal organs from developing lesions despite the presence of aggressive tumor cells.

Original languageEnglish
Pages (from-to)1833-1847
Number of pages15
JournalNature Biotechnology
Volume43
Issue number11
Early online dateNov 9 2024
DOIs
StatePublished - Nov 2025

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Animals
  • Cell Competition
  • Cell Line, Tumor
  • Exosomes/metabolism
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Mice
  • Ovarian Neoplasms/pathology
  • RNA, Long Noncoding/genetics
  • Tumor Microenvironment/genetics

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