Evidence map›Paper›PMID 30290054›Full record

ArticleCancer science2018

Possible role of p53/Mieap-regulated mitochondrial quality control as a tumor suppressor in human breast cancer.

Siqin Gaowa, Manabu Futamura, Masayuki Tsuneki, Hiroki Kamino, Jesse Y Tajima, Ryutaro Mori, Hirofumi Arakawa, Kazuhiro Yoshida

Abstract read
In one paragraph

Article in Cancer science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
–field-weighted citation impact
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

14 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. The emerging mechanisms and functions of microautophagy.Nature reviews. Molecular cell biology · 2023
    Review
  6. High SPATA18 Expression and its Diagnostic and Prognostic Value in Clear Cell Renal Cell Carcinoma.Medical science monitor : international medical journal of experimental and clinical research · 2023
    Article
  7. Article
  8. Article
  9. American journal of cancer research · 2021
    Article
  10. Article
  11. Review
  12. Article
  13. How DNA methylation affects the Warburg effect.International journal of biological sciences · 2020
    Review
  14. 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

8 authors.

Siqin GaowaDepartment of Surgical Oncology, Graduate School of Medicine, Gifu University, Gifu, Japan.
Manabu FutamuraDepartment of Surgical Oncology, Graduate School of Medicine, Gifu University, Gifu, Japan.ORCID http://orcid.org/0000-0001-5622-8352
Masayuki TsunekiDivision of Cancer Biology, National Cancer Center Research Institute, Tokyo, Japan.
Hiroki KaminoDivision of Cancer Biology, National Cancer Center Research Institute, Tokyo, Japan.
Jesse Y TajimaDepartment of Surgical Oncology, Graduate School of Medicine, Gifu University, Gifu, Japan.
Ryutaro MoriDepartment of Surgical Oncology, Graduate School of Medicine, Gifu University, Gifu, Japan.
Hirofumi ArakawaDivision of Cancer Biology, National Cancer Center Research Institute, Tokyo, Japan.ORCID http://orcid.org/0000-0001-6077-0638
Kazuhiro YoshidaDepartment of Surgical Oncology, Graduate School of Medicine, Gifu University, Gifu, Japan.

Funding

AMED 15ck0106006 h0002 (to HA)KAKENIHI 17K10542 (to MF)KAKENIHI 23659178 (to HA)KAKENIHI 24240117 (to HA)KAKENIHI 25670169 (to HA)Ministry of Health, Labour and Welfare for the Practical Research for Innovative Cancer H26-practical-general-001 (to HA)The National Cancer Center Research and Development Fund 29-E-1 (to HA), 30-A-3 (to HA)
6 · The paper itself

Abstract

Mitochondria-eating protein (Mieap), encoded by a p53-target gene, plays an important role in mitochondrial quality control (MQC). Mieap has been reported to have a critical role in tumor suppression in colorectal cancer. Here, we investigated its role as a tumor suppressor in breast cancer. The enforced expression of exogenous Mieap in breast cancer cells induced caspase-dependent apoptosis, with activation of both caspase-3/7 and caspase-9. Immunohistochemistry revealed endogenous Mieap in the cytoplasm in 24/75 (32%) invasive ductal carcinomas (IDC), 15/27 (55.6%) cases of ductal carcinoma in situ (DCIS) and 16/18 (88.9%) fibroadenomas (FA) (IDC vs DCIS; P = 0.0389, DCIS vs FA; P = 0.0234, IDC vs FA; P < 0.0001). In IDC, the Mieap promoter was methylated in 6/46 (13%) cases, whereas p53 was mutated in 6/46 (13%) cases. Therefore, the p53/Mieap-regulated MQC pathway was inactivated in 12/46 IDC (26.1%). Interestingly, all tumors derived from the 12 patients with Mieap promoter methylation or p53 mutations pathologically exhibited more aggressive and malignant breast cancer phenotypes. Impairment of p53/Mieap-regulated MQC pathway resulted in significantly shorter disease-free survival (DFS) (P = 0.021), although p53 status is more prognostic in DFS than Mieap promoter methylation. These results indicate that p53/Mieap-regulated MQC has a critical role in tumor suppression in breast cancer, possibly in part through mitochondrial apoptotic pathway.

Indexed as

AdultAgedAged, 80 and overApoptosisBreast NeoplasmsCarcinoma, Ductal, BreastCaspasesCell Line, TumorCytoplasmDisease-Free SurvivalDNA MethylationFemaleGene Expression Regulation, NeoplasticHumansMCF-7 CellsMiddle AgedCaspasesMitochondrial ProteinsSPATA18 protein, humanTP53 protein, humanTumor Suppressor Protein p53apoptosisbreast cancercaspaseMieappromoter methylation

Identifiers

PMID30290054
PMCPMC6272104

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.