Evidence map›Paper›PMID 31992715›Full record

ArticleNature communications2020

HSP90A inhibition promotes anti-tumor immunity by reversing multi-modal resistance and stem-like property of immune-refractory tumors.

Kwon-Ho Song, Se Jin Oh, Suyeon Kim, Hanbyoul Cho, Hyo-Jung Lee, Joon Seon Song, Joon-Yong Chung, Eunho Cho, Jaeyoon Lee, Seunghyun Jeon and 6 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 2 pooled it
4.8field-weighted citation impact, top 4% 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

59 citing papers in PubMed, 2 syntheses or guidelines pooled it, 94 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Tumor cell intrinsic mechanisms of immune escape.Cell communication and signaling : CCS · 2026
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 5 institutions in 3 countries.

Kwon-Ho Song *Department of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0001-6547-1143
Se Jin Oh *Department of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea.
Suyeon Kim *Department of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-3691-7692
Hanbyoul ChoDepartment of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Hyo-Jung LeeDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea.
Joon Seon SongExperimental Pathology Laboratory, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.
Joon-Yong ChungExperimental Pathology Laboratory, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.ORCID http://orcid.org/0000-0001-5041-5982
Eunho ChoDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea.
Jaeyoon LeeCollege of Science, College of Social Sciences and Humanities, Northeastern University, Boston, MA, USA.ORCID http://orcid.org/0000-0002-5231-0284
Seunghyun JeonDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-4320-2644
Cassian YeeDepartment of Gynecologic Oncology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Kyung-Mi LeeDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea.ORCID http://orcid.org/0000-0002-5378-9258
Stephen M HewittExperimental Pathology Laboratory, Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, 20892, USA.ORCID http://orcid.org/0000-0001-8283-1788
Jae-Hoon KimDepartment of Obstetrics and Gynecology, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Seon Rang WooDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea. na26012601@korea.ac.kr.
Tae Woo KimDepartment of Biochemistry & Molecular Biology, Korea University College of Medicine, Seoul, Korea. twkim0421@korea.ac.kr.
Korea University · KRNational Institutes of Health · USYonsei University · KRNortheastern University · USThe University of Texas MD Anderson Cancer Center · US

Funding

National Research Foundation of Korea (NRF) NRF-2016R1A6A3A11933484National Research Foundation of Korea (NRF) NRF-2019R1A4A1029000
6 · The paper itself

Abstract

Cancer immunotherapy has emerged as a promising cancer treatment. However, the presence of immune-refractory tumor cells limits its clinical success by blocking amplification of anti-tumor immunity. Previously, we found that immune selection by immunotherapy drives the evolution of tumors toward multi-modal resistant and stem-like phenotypes via transcription induction of AKT co-activator TCL1A by NANOG. Here, we report a crucial role of HSP90A at the crossroads between NANOG-TCL1A axis and multi-aggressive properties of immune-edited tumor cells by identifying HSP90AA1 as a NANOG transcriptional target. Furthermore, we demonstrate that HSP90A potentiates AKT activation through TCL1A-stabilization, thereby contributing to the multi-aggressive properties in NANOG

Indexed as

ImmunityImmunotherapyAnimalsCell Line, TumorFemaleHSP90 Heat-Shock ProteinsHumansIsoxazolesMice, Inbred C57BLMice, Inbred NODMice, SCIDNanog Homeobox ProteinNeoplastic Stem CellsProgrammed Cell Death 1 ReceptorProto-Oncogene ProteinsProto-Oncogene Proteins c-akt5-(2,4-dihydroxy-5-isopropylphenyl)-4-(4-morpholin-4-ylmethylphenyl)isoxazole-3-carboxylic acid ethylamideHSP90AA1 protein, humanHSP90 Heat-Shock ProteinsIsoxazolesNanog Homeobox ProteinNANOG protein, humanPDCD1 protein, humanProgrammed Cell Death 1 ReceptorProto-Oncogene ProteinsProto-Oncogene Proteins c-aktResorcinolsTCL1A protein, human

Identifiers

PMID31992715
PMCPMC6987099
OpenAlexW3004034317

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.