Literature DB >> 29563136

The Pattern of Mesenchymal Stem Cell Expression Is an Independent Marker of Outcome in Multiple Myeloma.

Carolina Schinke1, Pingping Qu2, Syed J Mehdi3, Antje Hoering2, Joshua Epstein3, Sarah K Johnson3, Frits van Rhee3, Maurizio Zangari3, Sharmilan Thanendrarajan3, Bart Barlogie3, Faith E Davies3, Shmuel Yaccoby1, Gareth J Morgan1.   

Abstract

Purpose: Mesenchymal stem cells (MSC) are an essential component of the bone marrow microenvironment and have shown to support cancer evolution in multiple myeloma. Despite the increasing evidence that multiple myeloma MSCs differ from their healthy counterparts, little knowledge exists as to whether MSCs independently influence disease outcome. The aim of this study was to determine the importance of MSCs in disease progression and outcome in multiple myeloma.Experimental Design: To determine the impact of MSCs on multiple myeloma outcome in an in vivo system, we first identified genes from cultured MSCs that were specific to MSC expression and were not or minimally expressed in plasma cells (PC) or other cells present in bone marrow aspirates. We then applied this MSC gene signature to whole bone marrow biopsies of multiple myeloma patients compared with healthy controls and determined MSC expression scores specific to multiple myeloma and predictive of outcome.
Results: We show that multiple myeloma MSC gene expression signatures can differentiate multiple myeloma from monoclonal gammopathy and smoldering multiple myeloma (SMM) as well as from healthy controls and treated multiple myeloma patients who have achieved a complete remission. We identified a prognostic gene score based on three MSC specific genes, COL4A1, NPR3 and ITGBL1, that was able to predict progression-free survival in multiple myeloma patients and progression into multiple myeloma from SMM.Conclusions: Our findings show that progression of multiple myeloma and of SMM into multiple myeloma does not rely solely on intrinsic PC factors, but is independently affected by the biology of the surrounding microenvironment. Clin Cancer Res; 24(12); 2913-9. ©2018 AACR. ©2018 American Association for Cancer Research.

Entities:  

Mesh:

Substances:

Year:  2018        PMID: 29563136     DOI: 10.1158/1078-0432.CCR-17-2627

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  8 in total

1.  Mesenchymal stem cells gene signature in high-risk myeloma bone marrow linked to suppression of distinct IGFBP2-expressing small adipocytes.

Authors:  Syed J Mehdi; Sarah K Johnson; Joshua Epstein; Maurizio Zangari; Pingping Qu; Antje Hoering; Frits van Rhee; Carolina Schinke; Sharmilan Thanendrarajan; Bart Barlogie; Faith E Davies; Gareth J Morgan; Shmuel Yaccoby
Journal:  Br J Haematol       Date:  2018-11-08       Impact factor: 6.998

2.  Bone marrow-derived mesenchymal stem cells inhibit CD8+ T cell immune responses via PD-1/PD-L1 pathway in multiple myeloma.

Authors:  Z Liu; F Mi; M Han; M Tian; L Deng; N Meng; J Luo; R Fu
Journal:  Clin Exp Immunol       Date:  2021-05-07       Impact factor: 5.732

3.  Mesenchymal Stem Cells Inhibit the Effects of Dexamethasone in Multiple Myeloma Cells.

Authors:  Mingyang Deng; Huan Yuan; Hongling Peng; Sufang Liu; Xiang Xiao; Zhihua Wang; Guangsen Zhang; Han Xiao
Journal:  Stem Cells Int       Date:  2022-04-04       Impact factor: 5.443

4.  Mesenchymal stem cells from bone marrow regulate invasion and drug resistance of multiple myeloma cells by secreting chemokine CXCL13.

Authors:  Guihua Zhang; Faan Miao; Jinge Xu; Rui Wang
Journal:  Bosn J Basic Med Sci       Date:  2020-05-01       Impact factor: 3.363

5.  ITGBL1 promotes EMT, invasion and migration by activating NF-κB signaling pathway in prostate cancer.

Authors:  Wenze Li; Shuren Li; Jie Yang; Chunyan Cui; Miao Yu; Yadong Zhang
Journal:  Onco Targets Ther       Date:  2019-05-16       Impact factor: 4.147

6.  Inhibiting PI3K-AKT-mTOR Signaling in Multiple Myeloma-Associated Mesenchymal Stem Cells Impedes the Proliferation of Multiple Myeloma Cells.

Authors:  Luca Heinemann; Klara Maria Möllers; Helal Mohammed Mohammed Ahmed; Lanying Wei; Kaiyan Sun; Subbaiah Chary Nimmagadda; Daria Frank; Anja Baumann; Alexandra M Poos; Martin Dugas; Julian Varghese; Marc-Steffen Raab; Cyrus Khandanpour
Journal:  Front Oncol       Date:  2022-06-20       Impact factor: 5.738

Review 7.  Multi-omics tumor profiling technologies to develop precision medicine in multiple myeloma.

Authors:  Sara Ovejero; Jerome Moreaux
Journal:  Explor Target Antitumor Ther       Date:  2021-02-28

8.  CXCL12/CXCR4 axis supports mitochondrial trafficking in tumor myeloma microenvironment.

Authors:  Cesarina Giallongo; Ilaria Dulcamare; Francesco Di Raimondo; Giuseppe A Palumbo; Daniele Tibullo; Vittorio Del Fabro; Nunzio Vicario; Nunziatina Parrinello; Alessandra Romano; Grazia Scandura; Giacomo Lazzarino; Concetta Conticello; Giovanni Li Volti; Angela Maria Amorini; Giuseppe Musumeci; Michelino Di Rosa; Francesca Polito; Rosaria Oteri; M'hammed Aguennouz; Rosalba Parenti
Journal:  Oncogenesis       Date:  2022-01-21       Impact factor: 7.485

  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.