Evidence map›Paper›PMID 37205191›Full record

ReviewFrontiers in oncology2023

The key role of microRNA-766 in the cancer development.

Jitendra Gupta, Hussein Riyadh Abdul Kareem Al-Hetty, Murtadha Sh Aswood, Abduladheem Turki Jalil, Maha Dhurgham Azeez, Zafar Aminov, Fahad Alsaikhan, Andrés Alexis Ramírez-Coronel, Pushpamala Ramaiah, Bagher Farhood

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. 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

10 authors at 10 institutions in 7 countries.

Jitendra GuptaInstitute of Pharmaceutical Research, GLA University, Mathura, India.
Hussein Riyadh Abdul Kareem Al-HettyDepartment of Nursing, Al-Maarif University College, Ramadi, Anbar, Iraq.
Murtadha Sh AswoodDepartment of Physics, College of Education, University of Al-Qadisiyah, Al-Diwaniyah, Iraq.
Abduladheem Turki JalilMedical Laboratories Techniques Department, Al-Mustaqbal University College, Babylon, Hilla, Iraq.
Maha Dhurgham AzeezNational University of Science and Technology, Dhi Qar, Iraq.
Zafar AminovDepartment of Public Health and Healthcare management, Samarkand State Medical University, Samarkand, Uzbekistan.
Fahad AlsaikhanCollege of Pharmacy, Prince Sattam Bin Abdulaziz University, Alkharj, Saudi Arabia.
Andrés Alexis Ramírez-CoronelAzogues Campus Nursing Career, Health and Behavior Research Group (HBR), Psychometry and Ethology Laboratory, Catholic University of Cuenca, Cuenca, Ecuador.
Pushpamala RamaiahFaculty of Nursing, Umm al-Qura University, Makkah, Saudi Arabia.
Bagher FarhoodDepartment of Medical Physics and Radiology, Faculty of Paramedical Sciences, Kashan University of Medical Sciences, Kashan, Iran.
Alsalam University College · IQGLA University · INKashan University of Medical Sciences · IRPrince Sattam Bin Abdulaziz University · SASamarkand State Medical Institute · UZThi Qar University · IQUmm al-Qura University · SAUniversidad Católica de Cuenca · ECUniversity of Al Maarif · IQUniversity of Al-Qadisiyah · IQ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer is caused by defects in coding and non-coding RNAs. In addition, duplicated biological pathways diminish the efficacy of mono target cancer drugs. MicroRNAs (miRNAs) are short, endogenous, non-coding RNAs that regulate many target genes and play a crucial role in physiological processes such as cell division, differentiation, cell cycle, proliferation, and apoptosis, which are frequently disrupted in diseases such as cancer. MiR-766, one of the most adaptable and highly conserved microRNAs, is notably overexpressed in several diseases, including malignant tumors. Variations in miR-766 expression are linked to various pathological and physiological processes. Additionally, miR-766 promotes therapeutic resistance pathways in various types of tumors. Here, we present and discuss evidence implicating miR-766 in the development of cancer and treatment resistance. In addition, we discuss the potential applications of miR-766 as a therapeutic cancer target, diagnostic biomarker, and prognostic indicator. This may shed light on the development of novel therapeutic strategies for cancer therapy.

Indexed as

biomarkercancerdrug resistancemicroRNAmiR-766

Identifiers

PMID37205191
PMCPMC10185842
OpenAlexW4367853488

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.