Evidence map›Paper›PMID 32167126›Full record

ArticleGenetics and molecular biology2020

Targeting STAT-3 signaling pathway in cancer for development of novel drugs: Advancements and challenges.

Sundas Arshad, Muhammad Naveed, Mahad Ullia, Khadija Javed, Ayesha Butt, Masooma Khawar, Fazeeha Amjad

Abstract read
In one paragraph

Article in Genetics and molecular biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

  1. Review
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  3. Article
  4. Innate immune role of IL-6 in influenza a virus pathogenesis.Frontiers in cellular and infection microbiology · 2025
    Review
  5. Review
  6. Article
  7. Article
  8. Article
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  11. Review
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  13. Article
  14. Article
  15. Tumor reversion: a dream or a reality.Biomarker research · 2021
    Review
  16. Article
  17. 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.

Sundas ArshadUniversity of Lahore, Department of Allied Health Sciences, Gujrat Campus, Pakistan.ORCID http://orcid.org/0000-0002-1165-2114
Muhammad NaveedUniversity of Central Punjab, Faculty of life sciences, Department of Biotechnology, Lahore, Pakistan.
Mahad UlliaUniversity of Gujrat, Department of Biochemistry and Biotechnology Sialkot sub Campus, Pakistan.
Khadija JavedUniversity of Gujrat, Department of Biochemistry and Biotechnology Sialkot sub Campus, Pakistan.
Ayesha ButtUniversity of Gujrat, Department of Biochemistry and Biotechnology Sialkot sub Campus, Pakistan.
Masooma KhawarUniversity of Gujrat, Department of Biochemistry and Biotechnology Sialkot sub Campus, Pakistan.
Fazeeha AmjadUniversity of Gujrat, Department of Biochemistry and Biotechnology Sialkot sub Campus, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Signal transducers and activators of transcription 3 (STAT-3) is a transcription factor that regulates the gene expression of several target genes. These factors are activated by the binding of cytokines and growth factors with STAT-3 specific receptors on cell membrane. Few years ago, STAT-3 was considered an acute phase response element having several cellular functions such as inflammation, cell survival, invasion, metastasis and proliferation, genetic alteration, and angiogenesis. STAT-3 is activated by several types of inflammatory cytokines, carcinogens, viruses, growth factors, and oncogenes. Thus, the STAT3 pathway is a potential target for cancer therapeutics. Abnormal STAT-3 activity in tumor development and cellular transformation can be targeted by several genomic and pharmacological methodologies. An extensive review of the literature has been conducted to emphasize the role of STAT-3 as a unique cancer drug target. This review article discusses in detail the wide range of STAT-3 inhibitors that show antitumor effects both in vitro and in vivo. Thus, targeting constitutive STAT-3 signaling is a remarkable therapeutic methodology for tumor progression. Finally, current limitations, trials and future perspectives of STAT-3 inhibitors are also critically discussed.

Identifiers

PMID32167126
PMCPMC7198026

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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.