Evidence map›Paper›PMID 32080166›Full record

ArticleCell death & disease2020

ID1 confers cancer cell chemoresistance through STAT3/ATF6-mediated induction of autophagy.

Jiao Meng, Kaiyi Liu, Yang Shao, Xu Feng, Zhaodong Ji, Bin Chang, Yan Wang, Ling Xu, Gong Yang

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
9.2field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 95 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. CD47 peptide-cloaked lipid nanoparticles promote cell-specific mRNA delivery.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Autophagy-mediated ID1 turnover dictates chemo-resistant fate in ovarian cancer stem cells.Journal of experimental & clinical cancer research : CR · 2024
    Article
  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

9 authors at 3 institutions in 1 country.

Jiao Meng *Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Kaiyi Liu *Department of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Yang Shao *Cancer Institute, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Xu FengCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Zhaodong JiCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, 200032, China.
Bin ChangDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Yan WangDepartment of Oncology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.
Ling XuDepartment of Obstetrics and Gynecology, Minhang Hospital, Fudan University, Shanghai, 201199, China. edelweiss76@163.com.
Gong YangCancer Institute, Fudan University Shanghai Cancer Center, Shanghai, 200032, China. yanggong@fudan.edu.cn.
Shanghai Medical College of Fudan University · CNFudan University Shanghai Cancer Center · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemoresistance is one of the major reasons leading to ovarian cancer high mortality and poor survival. Studies have shown that the alteration of cellular autophagy is associated with cancer cell chemoresistance. Here, we investigated whether the ovarian cancer chemoresistance is associated with the autophagy induced by the inhibitor of DNA binding 1 (ID1). By using gene overexpression or silencing, luciferase assay and human specimens, we show that ID1 induces high autophagy and confers cancer cell chemoresistance. The mechanistic study demonstrates that ID1 first activates the NF-κB signaling through facilitating the nuclear translocation of NF-κB p65, which strengthens the expression and secretion of IL-6 from cancer cells to subsequently activate the signal transducer and activator of transcription 3 (STAT3) through the protein phosphorylation at Y705. We further identified that STAT3 functions to promote the transcription of the activating transcription factor 6 (ATF6), which induces endoplasmic reticulum stress to promote cellular autophagy, granting cancer cell resistance to both cisplatin and paclitaxel treatment. Moreover, we found a significant correlation between the expression of ID1 and ATF6 in 1104 high grade serous ovarian cancer tissues, and that patients with the high expression of ID1 or ATF6 were resistant to platinum treatment and had the poor overall survival and progression-free survival. Thus, we have uncovered a mechanism in which ID1 confers cancer cell chemoresistance largely through the STAT3/ATF6-induced autophagy. The involved molecules, including ID1, STAT3, and ATF6, may have a potential to be targeted in combination with chemotherapeutic agents to improve ovarian cancer survival.

Indexed as

AutophagyDrug Resistance, NeoplasmActivating Transcription Factor 6AnimalsAntineoplastic AgentsCell Line, TumorCisplatinFemaleGene Expression Regulation, NeoplasticHumansInhibitor of Differentiation Protein 1Interleukin-6Mice, Inbred BALB CMice, NudeNF-kappa BOvarian NeoplasmsActivating Transcription Factor 6Antineoplastic AgentsATF6 protein, humanCisplatinID1 protein, humanIL6 protein, humanInhibitor of Differentiation Protein 1Interleukin-6NF-kappa BPaclitaxelSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID32080166
PMCPMC7033197
OpenAlexW3007924348

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.