Evidence map›Paper›PMID 34769090›Full record

ReviewInternational journal of molecular sciences2021

Emerging Importance of Tyrosine Kinase Inhibitors against Cancer: Quo Vadis to Cure?

Raj Kumar Mongre, Chandra Bhushan Mishra, Arvind Kumar Shukla, Amresh Prakash, Samil Jung, Md Ashraf-Uz-Zaman, Myeong-Sok Lee

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

21 citing papers in PubMed, 36 citations in OpenAlex.

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  16. CSK-mediated signalling by integrins in cancer.Frontiers in cell and developmental biology · 2023
    Review
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  18. Discovery of new 1Journal of enzyme inhibition and medicinal chemistry · 2022
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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 at 4 institutions in 2 countries.

Raj Kumar MongreMolecular Cancer Biology Laboratory, Cellular Heterogeneity Research Center, Department of Biosystem, Sookmyung Women's University, Hyochangwon gil-52, Seoul 04310, Yongsan-gu, Korea.
Chandra Bhushan MishraDepartment of Pharmacology & Chemical Biology, Baylor College of Medicine, Baylor Plaza, Houston, TX 77030, USA.
Arvind Kumar ShuklaSchool of Biomedical Convergence Engineering, Pusan National University, Yangsan 50612, Gyeongsangnam-do, Korea.ORCID 0000-0002-9838-7842
Amresh PrakashAmity Institute of Integrative Sciences and Health (AIISH), Amity University Haryana, Gurgaon 122413, India.
Samil JungMolecular Cancer Biology Laboratory, Cellular Heterogeneity Research Center, Department of Biosystem, Sookmyung Women's University, Hyochangwon gil-52, Seoul 04310, Yongsan-gu, Korea.
Md Ashraf-Uz-ZamanDepartment of Pharmacology & Chemical Biology, Baylor College of Medicine, Baylor Plaza, Houston, TX 77030, USA.
Myeong-Sok LeeMolecular Cancer Biology Laboratory, Cellular Heterogeneity Research Center, Department of Biosystem, Sookmyung Women's University, Hyochangwon gil-52, Seoul 04310, Yongsan-gu, Korea.
Baylor College of Medicine · USSookmyung Women's University · KRPusan National University · KRUniversity of Rochester Medical Center · US

Funding

National Research Foundation of Korea funded by the Korean Government (MSIP) [Grant nos. NRF-2016R1A5A1011974 and NRF 2020R1A2C1102100.
6 · The paper itself

Abstract

GLOBOCAN 2020 estimated more than 19.3 million new cases, and about 10 million patients were deceased from cancer in 2020. Clinical manifestations showed that several growth factor receptors consisting of transmembrane and cytoplasmic tyrosine kinase (TK) domains play a vital role in cancer progression. Receptor tyrosine kinases (RTKs) are crucial intermediaries of the several cellular pathways and carcinogenesis that directly affect the prognosis and survival of higher tumor grade patients. Tyrosine kinase inhibitors (TKIs) are efficacious drugs for targeted therapy of various cancers. Therefore, RTKs have become a promising therapeutic target to cure cancer. A recent report shows that TKIs are vital mediators of signal transduction and cancer cell proliferation, angiogenesis, and apoptosis. In this review, we discuss the structure and function of RTKs to explore their prime role in cancer therapy. Various TKIs have been developed to date that contribute a lot to treating several types of cancer. These TKI based anticancer drug molecules are also discussed in detail, incorporating their therapeutic efficacy, mechanism of action, and side effects. Additionally, this article focuses on TKIs which are running in the clinical trial and pre-clinical studies. Further, to gain insight into the pathophysiological mechanism of TKIs, we also reviewed the impact of RTK resistance on TKI clinical drugs along with their mechanistic acquired resistance in different cancer types.

Indexed as

Molecular Targeted TherapyAnimalsAntineoplastic AgentsBinding SitesClinical Trials as TopicDrug Evaluation, PreclinicalHumansNeoplasmsProtein-Tyrosine KinasesAntineoplastic AgentsProtein-Tyrosine Kinasescancerclinical trialsdrug resistancemutationreceptor tyrosine kinasestargeted therapy

Identifiers

PMID34769090
PMCPMC8584061
OpenAlexW3209958427

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.