Evidence map›Paper›PMID 32802161›Full record

ReviewOncology letters2020

Long non-coding RNA regulation of TRAIL in breast cancer: A tangle of non-coding threads.

Zeeshan Javed, Khushbukhat Khan, Muhammad Zaheer Iqbal, Touqeer Ahmad, Qamar Raza, Haleema Sadia, Shahid Raza, Bahare Salehi, Javad Sharifi-Rad, William C Cho

Open access · diamondAbstract readReview
In one paragraph

Review in Oncology letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 50% 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

5 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Review
  5. 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

10 authors at 8 institutions in 3 countries.

Zeeshan JavedOffice for Research Innovation and Commercialization, Lahore Garrison University, Lahore, Punjab 54792, Pakistan.
Khushbukhat KhanAtta-ur-Rahman School of Applied Biosciences, National University of Sciences and Technology, Islamabad, Punjab 44000, Pakistan.
Muhammad Zaheer IqbalCenter for Excellence in Molecular Biology, University of the Punjab, Lahore, Punjab 53700, Pakistan.
Touqeer AhmadInstitute of Microbiology, University of Veterinary and Animal Sciences, Lahore, Punjab 54000, Pakistan.
Qamar RazaInstitute of Biochemistry and Biotechnology, University of Veterinary and Animal Sciences, Lahore, Punjab 54000, Pakistan.
Haleema SadiaDepartment of Biotechnology, Balochistan University of Information Technology, Engineering and Management Sciences, Quetta, Balochistan 87100, Pakistan.
Shahid RazaOffice for Research Innovation and Commercialization, Lahore Garrison University, Lahore, Punjab 54792, Pakistan.
Bahare SalehiNoncommunicable Diseases Research Center, Bam University of Medical Sciences, Bam 44340847, Iran.
Javad Sharifi-RadPhytochemistry Research Center, Shahid Beheshti University of Medical Sciences, Tehran 1991953381, Iran.
William C ChoDepartment of Clinical Oncology, Queen Elizabeth Hospital, Hong Kong SAR, P.R. China.
Lahore Garrison University · PKUniversity of Veterinary and Animal Sciences · PKBalochistan University of Information Technology, Engineering and Management Sciences · PKBam University of Medical Sciences · IRNational University of Sciences and Technology · PKQueen Elizabeth Hospital · CNShahid Beheshti University of Medical Sciences · IRUniversity of the Punjab · PK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is a complex disease posing a serious threat to the female population worldwide. A complex molecular landscape and tumor heterogeneity render breast cancer cells resistant to drugs and able to promote metastasis and invasiveness. Despite the recent advancements in diagnostics and drug discovery, finding an effective cure for breast cancer is still a major challenge. Positive and negative regulation of apoptosis has been a subject of extensive study over the years. Numerous studies have shed light on the mechanisms that impede the tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) signaling cascade. Long non-coding RNAs (lncRNAs) have been implicated in the orchestration, development, proliferation, differentiation and metastasis of breast cancer. However, the roles of lncRNAs in fine-tuning apoptosis regulating machinery in breast cancer remain to be elucidated. The present review illuminates the roles of these molecules in the regulation of breast cancer and the interplay between lncRNA and TRAIL in breast cancer. The present review also attempts to reveal their role in the regulation of apoptosis in breast cancer appears a promising approach for the development of new diagnostic and therapeutic regimens.

Indexed as

breast cancerdiagnosislong non-coding RNAtherapeuticstumor necrosis factor-related apoptosis-inducing ligand

Identifiers

PMID32802161
PMCPMC7412712
OpenAlexW3044569360

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.