Evidence map›Paper›PMID 21437292›Full record

ArticlePloS one2011

Chemotherapy-induced late transgenerational effects in mice.

Loro L Kujjo, Eun A Chang, Ricardo J G Pereira, Shilpa Dhar, Brenda Marrero-Rosado, Satyaki Sengupta, Hongbing Wang, Jose B Cibelli, Gloria I Perez

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
5.7field-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

20 citing papers in PubMed, 51 citations in OpenAlex.

  1. Article
  2. Review
  3. AMH protects the ovary from doxorubicin by regulating cell fate and the response to DNA damage.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Environmental epigenetics and phytoestrogen/phytochemical exposures.The Journal of steroid biochemistry and molecular biology · 2014
    Review
  16. Article
  17. Review
  18. Experimental evidence showing that no mitotically active female germline progenitors exist in postnatal mouse ovaries.Proceedings of the National Academy of Sciences of the United States of America · 2012
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Loro L KujjoDepartment of Physiology, Michigan State University, East Lansing, Michigan, United States of America.
Eun A Chang
Ricardo J G Pereira
Shilpa Dhar
Brenda Marrero-Rosado
Satyaki Sengupta
Hongbing Wang
Jose B Cibelli
Gloria I Perez
Michigan State University · USMichigan United · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To our knowledge, there is no report on long-term reproductive and developmental side effects in the offspring of mothers treated with a widely used chemotherapeutic drug such as doxorubicin (DXR), and neither is there information on transmission of any detrimental effects to several filial generations. Therefore, the purpose of the present paper was to examine the long-term effects of a single intraperitoneal injection of DXR on the reproductive and behavioral performance of adult female mice and their progeny. C57BL/6 female mice (generation zero; G0) were treated with either a single intraperitoneal injection of DXR (G0-DXR) or saline (G0-CON). Data were collected on multiple reproductive parameters and behavioral analysis for anxiety, despair and depression. In addition, the reproductive capacity and health of the subsequent six generations were evaluated. G0-DXR females developed despair-like behaviors; delivery complications; decreased primordial follicle pool; and early lost of reproductive capacity. Surprisingly, the DXR-induced effects in oocytes were transmitted transgenerationally; the most striking effects being observed in G4 and G6, constituting: increased rates of neonatal death; physical malformations; chromosomal abnormalities (particularly deletions on chromosome 10); and death of mothers due to delivery complications. None of these effects were seen in control females of the same generations. Long-term effects of DXR in female mice and their offspring can be attributed to genetic alterations or cell-killing events in oocytes or, presumably, to toxicosis in non-ovarian tissues. Results from the rodent model emphasize the need for retrospective and long-term prospective studies of survivors of cancer treatment and their offspring.

Indexed as

AnimalsAntineoplastic AgentsAnxietyAtrophybcl-2-Associated X ProteinBehavior, AnimalChromosome DeletionChromosomes, MammalianDoxorubicinFemaleHeredityHumansLysophospholipidsMaleMiceMice, Inbred C57BLAntineoplastic Agentsbcl-2-Associated X ProteinDoxorubicinLysophospholipidsSphingosinesphingosine 1-phosphate

Identifiers

PMID21437292
PMCPMC3060098
OpenAlexW2091613175

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.