Evidence map›Paper›PMID 31436298›Full record

ReviewOncology reports2019

Autophagy modulation in bladder cancer development and treatment (Review).

Faping Li, Hui Guo, Yuxuan Yang, Mingliang Feng, Bin Liu, Xiang Ren, Honglan Zhou

Abstract readReview
In one paragraph

Review in Oncology reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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

38 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. NR4A3 suppresses bladder cancer progression by modulating autophagyEuropean journal of histochemistry : EJH · 2025
    Article
  5. Article
  6. HomogeneousPharmaceutical biology · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Frontiers in cellular and infection microbiology · 2023
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  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.

Faping LiDepartment of Urology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Hui GuoDepartment of Urology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Yuxuan YangDepartment of Urology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Mingliang FengDepartment of Urology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Bin LiuDepartment of Urology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Xiang RenDepartment of Urology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.
Honglan ZhouDepartment of Urology, The First Hospital of Jilin University, Changchun, Jilin 130021, P.R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bladder cancer (BC) is a potentially life‑threatening malignancy. Due to a high recurrence rate, frequent surveillance strategies and intravesical drug therapies, BC is considered one of the most expensive tumors to treat. As a fundamental evolutionary catabolic process, autophagy plays an important role in the maintenance of cellular environmental homeostasis by degrading and recycling damaged cytoplasmic components, including macromolecules and organelles. Scientific studies in the last two decades have shown that autophagy acts as a double‑edged sword with regard to the treatment of cancer. On one hand, autophagy inhibition is able to increase the sensitivity of cancer cells to treatment, a process known as protective autophagy. On the other hand, autophagy overactivation may lead to cell death, referred to as autophagic cell death, similar to apoptosis. Therefore, it is essential to identify the role of autophagy in cancer cells in order to develop novel therapeutic agents. In addition, autophagy may potentially become a novel therapeutic target in human diseases. In this review, the current knowledge on autophagy modulation in BC development and treatment is summarized.

Indexed as

AutophagyApoptosisCell SurvivalGene Expression Regulation, NeoplasticHumansSignal TransductionUrinary Bladder Neoplasms

Identifiers

PMID31436298
PMCPMC6775810

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.