Evidence map›Paper›PMID 25712988›Full record

ArticleBlood2015

Tyrosine kinase inhibitors induce mesenchymal stem cell-mediated resistance in BCR-ABL+ acute lymphoblastic leukemia.

Saradhi Mallampati, Xiaohong Leng, Haiqing Ma, Jianfang Zeng, June Li, Haiying Wang, Kevin Lin, Yue Lu, Yang Yang, Baohua Sun and 15 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
3.8field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

20 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Article
  7. Galectin-1 and Galectin-3 in B-Cell Precursor Acute Lymphoblastic Leukemia.International journal of molecular sciences · 2022
    Article
  8. Review
  9. CD90Stem cell research & therapy · 2021
    Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 6 institutions in 2 countries.

Saradhi MallampatiDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and.
Xiaohong LengDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX;
Haiqing MaDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and Department of Oncology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, China;
Jianfang ZengDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and.
June LiDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and.
Haiying WangDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and Department of Hematology, The Affiliated Hospital of Weifang Medical University, Weifang, Shandong, China;
Kevin LinDepartment of Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, TX;
Yue LuDepartment of Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Houston, TX;
Yang YangDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and Multiple Myeloma Treatment Center and Department of Hematology, The First Affiliated Hospital of Medical College, Zhejiang University, Hangzhou, Zhejiang, China;
Baohua SunDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and.
Yun GongDepartment of Pathology.
Ju-Seog LeeDepartment of System Biology.
Marina KonoplevaDepartment of Leukemia, Department of Stem Cell Transplantation, and.
Michael AndreeffDepartment of Leukemia, Department of Stem Cell Transplantation, and.
Ralph B ArlinghausDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX;
Zhen CaiMultiple Myeloma Treatment Center and Department of Hematology, The First Affiliated Hospital of Medical College, Zhejiang University, Hangzhou, Zhejiang, China;
Bingliang FangDepartment of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Houston, TX;
Haifa ShenDepartment of Nanomedicine, Houston Methodist Research Institute, Houston, TX; Department of Cell and Developmental Biology, Weill Cornell Medical College, New York, NY; and.
Xin HanDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and.
Cheryl F Hirsch-GinsbergDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and.
Xiaolian GaoDepartment of Biology and Biochemistry, University of Houston, Houston, TX.
Anurag N ParanjapeDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX;
Sendurai A ManiDepartment of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX;
Karen Clise-DwyerDepartment of Stem Cell Transplantation, and.
Xiaoping SunDepartment of Laboratory Medicine and the Center for Stem Cell and Developmental Biology, and.
The University of Texas MD Anderson Cancer Center · USFirst Affiliated Hospital Zhejiang University · CNCornell University · USSun Yat-sen University · CNUniversity of Houston · USWeifang Medical University · CN

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI DIANE BODURKA · 1985 to 2026
$290.8M
Study Sox4 regulated genes in B cell development in a novel in vitro systemR21AI103652 · NIAID · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI SUN, XIAOPING · 2014 to 2015
$440k
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672NIAID NIH HHS 1R21AI103652-01A1NIAID NIH HHS R21 AI103652
6 · The paper itself

Abstract

Tyrosine kinase inhibitors (TKIs) are used as a frontline therapy for BCR-ABL(+) acute lymphoblastic leukemia (ALL). However, resistance to TKI therapy arises rapidly, and its underlying molecular mechanisms are poorly understood. In this study, we identified a novel cascade of events initiated by TKIs and traversing through mesenchymal stem cells (MSCs) to leukemic cells, leading to resistance. MSCs exposed to TKIs acquired a new functional status with the expression of genes encoding for chemo-attractants, adhesion molecules, and prosurvival growth factors, and this priming enabled leukemic cells to form clusters underneath the MSCs. This cluster formation was associated with the protection of ALL cells from therapy as leukemic cells switched from BCR-ABL signaling to IL-7R/Janus kinase signaling to survive in the MSC milieu. Our findings illustrate a novel perspective in the evolution of TKI resistance and provide insights for advancing the treatment of BCR-ABL(+) ALL.

Indexed as

Drug Resistance, NeoplasmAnimalsBiomarkers, TumorCell Transformation, NeoplasticFusion Proteins, bcr-ablGene Expression ProfilingMesenchymal Stem CellsMiceOligonucleotide Array Sequence AnalysisPrecursor Cell Lymphoblastic Leukemia-LymphomaProtein Kinase InhibitorsSignal TransductionTumor Cells, CulturedBiomarkers, TumorFusion Proteins, bcr-ablProtein Kinase Inhibitors

Identifiers

PMID25712988
PMCPMC4424418
OpenAlexW1964882859

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.