Evidence map›Paper›PMID 29644941›Full record

ReviewCurrent cancer drug targets2018

Role of MicroRNAs in Treatment Response in Prostate Cancer.

Anshuli Razdan, Paul de Souza, Tara Laurine Roberts

Registry-linked trialAbstract readReview
In one paragraph

Review in Current cancer drug targets, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04662996 (Search for Predictive Factors of Resistance to Treatment for Metastatic Castration-resistant Prostate Cancer by Studying the Expression of microRNAs), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.1field-weighted citation impact, top 27% 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.

NCT04662996 nacompletednot on this mapstarted 2021, after this paper: background citation

Search for Predictive Factors of Resistance to Treatment for Metastatic Castration-resistant Prostate Cancer by Studying the Expression of microRNAs

TypeinterventionalSponsorUniversity Hospital, ToursRan2021 to 2023Enrolled33ConditionsProstate Cancer, Resistance, Disease, MicroRNAsArmsBlood sample
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Crucial Roles of microRNA-Mediated Autophagy in Urologic Malignancies.International journal of biological sciences · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. MiR-92a promotes the invasion and migration of colorectal cancer by targeting RECK.International journal of clinical and experimental pathology · 2019
    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

3 authors at 1 institution in 1 country.

Anshuli RazdanMedical Oncology Group, Ingham Institute for Applied Medical Research, Liverpool, New South Wales, Australia.
Paul de SouzaMedical Oncology Group, Ingham Institute for Applied Medical Research, Liverpool, New South Wales, Australia.
Tara Laurine RobertsMedical Oncology Group, Ingham Institute for Applied Medical Research, Liverpool, New South Wales, Australia.
Ingham Institute · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Prostate cancer (PCa) is the most common non-skin cancer in men worldwide, resulting in significant mortality and morbidity. Depending on the grade and stage of the cancer, patients may be given radiation therapy, hormonal therapy, or chemotherapy. However, more than half of these patients develop resistance to treatment, leading to disease progression and metastases, often with lethal consequences. MicroRNAs (miRNAs) are short, non-coding RNAs, which regulate numerous physiological as well as pathological processes, including cancer. miRNAs mediate their regulatory effect predominately by binding to the 3'-untranslated region (UTR) of their target mRNAs. In this review, we will describe the mechanisms by which miRNAs mediate resistance to radiation and drug therapy (i.e. hormone therapy and chemotherapy) in PCa, including control of apoptosis, cell growth and proliferation, autophagy, epithelial-to-mesenchymal transition (EMT), invasion and metastasis, and cancer stem cells (CSCs). Furthermore, we will discuss the utility of circulating miRNAs isolated from different body fluids of prostate cancer patients as non-invasive biomarkers of cancer detection, disease progression, and therapy response. Finally, we will shortlist the candidate miRNAs, which may have a role in drug and radioresistance, that could potentially be used as predictive biomarkers of treatment response.

Indexed as

AnimalsApoptosisBiomarkers, TumorBody FluidsDisease ProgressionDrug Resistance, NeoplasmHumansMaleMiceMicroRNAsProstatic Neoplasms, Castration-ResistantBiomarkers, TumorMicroRNAsapoptosisbiomarkersMicroRNAs (miRNAs)prostate cancerradiation and drug therapytherapy response.

Identifiers

PMID29644941
PMCPMC6463399
OpenAlexW2793989844

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.