Evidence map›Paper›PMID 29141221›Full record

ArticleCell reports2017

Chemotherapy-Induced Depletion of OCT4-Positive Cancer Stem Cells in a Mouse Model of Malignant Testicular Cancer.

Timothy M Pierpont, Amy M Lyndaker, Claire M Anderson, Qiming Jin, Elizabeth S Moore, Jamie L Roden, Alicia Braxton, Lina Bagepalli, Nandita Kataria, Hilary Zhaoxu Hu and 6 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

27 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. MicroRNAs in Testicular Germ Cell Tumors: The Teratoma Challenge.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. A Genetically Engineered Mouse Model of Malignant Testicular Germ Cell Tumors.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  18. Review
  19. Review
  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 3 institutions in 1 country.

Timothy M PierpontDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Amy M LyndakerDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA. Electronic address: alyndaker@elmira.edu.
Claire M AndersonDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Qiming JinDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Elizabeth S MooreDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Jamie L RodenDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Alicia BraxtonDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Lina BagepalliDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Nandita KatariaDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Hilary Zhaoxu HuDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Jason GarnessDepartment of Cell Biology, Duke University Medical Center, Durham, NC, USA.
Matthew S CookDepartment of Cell Biology, Duke University Medical Center, Durham, NC, USA.
Blanche CapelDepartment of Cell Biology, Duke University Medical Center, Durham, NC, USA.
Donald H SchlaferDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Teresa SouthardDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA.
Robert S WeissDepartment of Biomedical Sciences, College of Veterinary Medicine, Cornell University, Ithaca, NY, USA. Electronic address: rsw26@cornell.edu.
Cornell University · USDuke Medical Center · USDuke University Hospital · US

Funding

PREDOCTORAL TRAINING IN CELLULAR AND MOLECULAR BIOLOGYT32GM007273 · NIGMS · CORNELL UNIVERSITY ITHACA · PI BRETSCHER, ANTHONY P. · 1985 to 2019
$11.6M
Training Program in Developmental & Stem Cell BiologyT32HD040372 · NICHD · DUKE UNIVERSITY · PI Terry H Lechler · 2001 to 2026
$8.9M
Training Veterinarians for Careers in Biomedical ResearchT32OD011089 · OD · JOHNS HOPKINS UNIVERSITY · PI JOSEPH L MANKOWSKI · 2012 to 2026
$6.7M
Graduate Training Program in Comparative MedicineT32OD011000 · OD · CORNELL UNIVERSITY · PI Amanda Marjorie DE MESTRE · 2012 to 2026
$5.7M
Reproductive Sciences and Genomics Training ProgramT32HD052471 · NICHD · CORNELL UNIVERSITY · PI ROBERSON, MARK S · 2007 to 2016
$2.0M
STUDENTS IN HEALTH PROFESSIONAL SCHOOLST35AI007227 · NIAID · CORNELL UNIVERSITY ITHACA · PI PARKER, JOHN S, VAN DE WALLE, GERLINDE R. · 1985 to 2023
$1.2M
Regulation of Germ Cell Pluripotency Through The RNA-Binding Protein, DND1R01GM087500 · NIGMS · DUKE UNIVERSITY · PI CAPEL, BLANCHE · 2010 to 2013
$1.2M
(PQD2) Molecular Basis for the Chemosensitivity of Testicular Germ Cell CancersR21CA185256 · NCI · CORNELL UNIVERSITY · PI WEISS, ROBERT S · 2014 to 2015
$371k
NCI NIH HHS R21 CA185256NIAID NIH HHS T35 AI007227NICHD NIH HHS T32 HD040372NICHD NIH HHS T32 HD052471NIGMS NIH HHS R01 GM087500NIGMS NIH HHS T32 GM007273NIH HHS T32 OD011000NIH HHS T32 OD011089
6 · The paper itself

Abstract

Testicular germ cell tumors (TGCTs) are among the most responsive solid cancers to conventional chemotherapy. To elucidate the underlying mechanisms, we developed a mouse TGCT model featuring germ cell-specific Kras activation and Pten inactivation. The resulting mice developed malignant, metastatic TGCTs composed of teratoma and embryonal carcinoma, the latter of which exhibited stem cell characteristics, including expression of the pluripotency factor OCT4. Consistent with epidemiological data linking human testicular cancer risk to in utero exposures, embryonic germ cells were susceptible to malignant transformation, whereas adult germ cells underwent apoptosis in response to the same oncogenic events. Treatment of tumor-bearing mice with genotoxic chemotherapy not only prolonged survival and reduced tumor size but also selectively eliminated the OCT4-positive cancer stem cells. We conclude that the chemosensitivity of TGCTs derives from the sensitivity of their cancer stem cells to DNA-damaging chemotherapy.

Indexed as

AnimalsAntineoplastic AgentsApoptosisCarcinomaCell Transformation, NeoplasticCisplatinMaleMiceMice, Inbred C57BLNeoplastic Stem CellsOctamer Transcription Factor-3TeratomaTesticular NeoplasmsAntineoplastic AgentsCisplatinOctamer Transcription Factor-3Pou5f1 protein, mousecancer stem cellschemotherapyCSCsDDRDNA damage responseECembryonal carcinomatesticular germ cell tumorTGCT

Identifiers

PMID29141221
PMCPMC5695237
OpenAlexW2769567513

What OpenQuestion holds

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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.