Evidence map›Paper›PMID 28165047›Full record

ArticleScientific reports2017

Relevance of mortalin to cancer cell stemness and cancer therapy.

Chae-Ok Yun, Priyanshu Bhargava, Youjin Na, Jung-Sun Lee, Jihoon Ryu, Sunil C Kaul, Renu Wadhwa

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. The mitochondrial unfolded protein response (UPRJournal of hematology & oncology · 2022
    Review
  11. Article
  12. Review
  13. Article
  14. Mitochondrial chaperones in human health and disease.Free radical biology & medicine · 2022
    Review
  15. A pan-metazoan concept for adult stem cells: the wobbling Penrose landscape.Biological reviews of the Cambridge Philosophical Society · 2022
    Article
  16. Article
  17. Article
  18. Why is Mortalin a Potential Therapeutic Target for Cancer?Frontiers in cell and developmental biology · 2022
    Review
  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

7 authors at 2 institutions in 2 countries.

Chae-Ok YunDepartment of Bioengineering, College of Engineering, Hanyang University, 222 Wangsinmi-ro, Seongdong-gu, Seoul, Republic of Korea.
Priyanshu BhargavaDBT-AIST International Laboratory for Advanced Biomedicine (DAILAB), Biomedical Research Institute, National Institute of Advanced Industrial Science &Technology (AIST), Central 5-41, 1-1-1 Higashi, Tsukuba - 305 8565, Japan.
Youjin NaDepartment of Bioengineering, College of Engineering, Hanyang University, 222 Wangsinmi-ro, Seongdong-gu, Seoul, Republic of Korea.
Jung-Sun LeeDepartment of Bioengineering, College of Engineering, Hanyang University, 222 Wangsinmi-ro, Seongdong-gu, Seoul, Republic of Korea.
Jihoon RyuDBT-AIST International Laboratory for Advanced Biomedicine (DAILAB), Biomedical Research Institute, National Institute of Advanced Industrial Science &Technology (AIST), Central 5-41, 1-1-1 Higashi, Tsukuba - 305 8565, Japan.
Sunil C KaulDBT-AIST International Laboratory for Advanced Biomedicine (DAILAB), Biomedical Research Institute, National Institute of Advanced Industrial Science &Technology (AIST), Central 5-41, 1-1-1 Higashi, Tsukuba - 305 8565, Japan.
Renu WadhwaDBT-AIST International Laboratory for Advanced Biomedicine (DAILAB), Biomedical Research Institute, National Institute of Advanced Industrial Science &Technology (AIST), Central 5-41, 1-1-1 Higashi, Tsukuba - 305 8565, Japan.
National Institute of Advanced Industrial Science and Technology · JPHanyang University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mortalin/mtHsp70 is a member of Hsp70 family of proteins. Enriched in a large variety of cancers, it has been shown to contribute to the process of carcinogenesis by multiple ways including inactivation of tumor suppressor p53 protein, deregulation of apoptosis and activation of EMT signaling. In this study, we report that upregulation of mortalin contributes to cancer cell stemness. Several cancer cell stemness markers, such as ABCG2, OCT-4, CD133, ALDH1, CD9, MRP1 and connexin were upregulated in mortalin-overexpressing cells that showed higher ability to form spheroids. These cells also showed higher migration, and were less responsive to a variety of cancer chemotherapeutic drugs. Of note, knockdown of mortalin by specific shRNA sensitized these cells to all the drugs used in this study. We report that low doses of anti-mortalin molecules, MKT-077 and CAPE, also caused similar sensitization of cancer cells to chemotherapeutic drugs and hence are potential candidates for effective cancer chemotherapy.

Indexed as

Antineoplastic AgentsBiomarkers, TumorCaffeic AcidsCell LineCell Line, TumorHSP70 Heat-Shock ProteinsHumansNeoplasmsNeoplastic Stem CellsPhenylethyl AlcoholPyridinesRNA, Small InterferingThiazolesUp-RegulationAntineoplastic AgentsBiomarkers, Tumorcaffeic acid phenethyl esterCaffeic AcidsHSP70 Heat-Shock ProteinsMKT 077mortalinPhenylethyl AlcoholPyridinesRNA, Small InterferingThiazoles

Identifiers

PMID28165047
PMCPMC5292728
OpenAlexW2587761286

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.