Evidence map›Paper›PMID 20552226›Full record

ArticleJournal of cancer research and clinical oncology2011

Evaluating mitochondrial DNA in patients with breast cancer and benign breast disease.

Lijun Shen, Jia Wei, Tao Chen, Jing He, Jianchun Qu, Xiumei He, Luxi Jiang, Yemin Qu, Hezhi Fang, Guorong Chen and 2 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

21 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Mitochondria in cancer.Cell stress · 2020
    Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Antibody Therapeutics in Oncology.Immunotherapy (Los Angeles, Calif.) · 2016
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Mitochondrial DNA mutations and breast tumorigenesis.Biochimica et biophysica acta · 2013
    Review
  14. Article
  15. Impaired mitochondrial metabolism and mammary carcinogenesis.Journal of mammary gland biology and neoplasia · 2013
    Review
  16. Article
  17. Review
  18. Physiology and pathophysiology of mitochondrial DNA.Advances in experimental medicine and biology · 2012
    Review
  19. Article
  20. Article
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

12 authors at 2 institutions in 2 countries.

Lijun ShenZhejiang Provincial Key Laboratory of Medical Genetics, Wenzhou Medical College, Wenzhou 325000, China.
Jia Wei
Tao Chen
Jing He
Jianchun Qu
Xiumei He
Luxi Jiang
Yemin Qu
Hezhi Fang
Guorong Chen
Jianxin Lu
Yidong Bai
Wenzhou Medical University · CNThe University of Texas Health Science Center at San Antonio · US

Funding

Role of Mitochondrial DNA Mutations in Aging in Neuronal CellsR01AG025223 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI BAI, YIDONG · 2006 to 2010
$1.4M
NIA NIH HHS R01 AG025223NIA NIH HHS R01AG025223
6 · The paper itself

Abstract

purposeTo evaluate the role of mtDNA in breast cancer.

methodsWe carried out an investigation into the mtDNA major control region or D-loop region and an essential and the largest mtDNA protein-coding gene, NADH dehydrogenase subunit 5 (ND5), together with a mitochondrial haplogroup analysis in 64 patients with breast cancer (BC) and 54 patients with benign breast disease (BBD) as controls.

resultsMutations in D-loop region were found in 10/64 or 15.6% of patients with BC and 14/54 or 25.9% of patients with BBD, while mutations in ND5 were detected in 6/64 or 9.4% of patients with BC and 5/54 or 9.3% of patients with BBD. In addition, in patients with BBD, mtDNA mutations were more likely to rise in D-loop region and the mutations were more likely to be heteroplasmic. However, in patients with BC, those with metastatic feature were less likely to carry mutations in D-loop region. Finally, we found haplogroup M has an increased risk of breast cancer compared with haplogroup N.

conclusionmtDNA mutation may play a role in early stage of tumorigenesis, and mitochondrial haplogroup can also modulate breast cancer occurrence.

Indexed as

AdolescentAdultAgedBreast DiseasesBreast NeoplasmsDNA, MitochondrialElectron Transport Complex IFemaleHaplotypesHumansMiddle AgedMitochondrial ProteinsMutationDNA, MitochondrialElectron Transport Complex IMitochondrial ProteinsMT-ND5 protein, human

Identifiers

PMID20552226
PMCPMC11827960
OpenAlexW1969498623

What OpenQuestion 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 OpenQuestion graph.