Evidence map›Paper›PMID 37470921›Full record

ReviewMolecular diversity2024

An updated literature on BRAF inhibitors (2018-2023).

Lalmohan Maji, Ghanshyam Teli, Nulgumnalli Manjunathaiah Raghavendra, Sindhuja Sengupta, Rohit Pal, Abhishek Ghara, Gurubasavaraja Swamy Purawarga Matada

Abstract readReview
PubMed Publisher
In one paragraph

Review in Molecular diversity, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
3.4field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

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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 2 institutions in 2 countries.

Lalmohan MajiDepartment of Pharmaceutical Chemistry, Integrated Drug Discovery Centre, Acharya & BM Reddy College of Pharmacy, Bengaluru, Karnataka, India.ORCID http://orcid.org/0000-0003-1542-7253
Ghanshyam TeliDepartment of Pharmaceutical Chemistry, Integrated Drug Discovery Centre, Acharya & BM Reddy College of Pharmacy, Bengaluru, Karnataka, India.ORCID http://orcid.org/0000-0002-7418-6683
Nulgumnalli Manjunathaiah RaghavendraDepartment of Pharmaceutical Chemistry, College of Pharmaceutical Sciences, Dayananda Sagar University, Bengaluru, Karnataka, India.ORCID http://orcid.org/0000-0002-0846-012X
Sindhuja SenguptaDepartment of Pharmaceutical Chemistry, Integrated Drug Discovery Centre, Acharya & BM Reddy College of Pharmacy, Bengaluru, Karnataka, India.ORCID http://orcid.org/0000-0001-7739-9644
Rohit PalDepartment of Pharmaceutical Chemistry, Integrated Drug Discovery Centre, Acharya & BM Reddy College of Pharmacy, Bengaluru, Karnataka, India.ORCID http://orcid.org/0000-0002-2763-5757
Abhishek GharaDepartment of Pharmaceutical Chemistry, Integrated Drug Discovery Centre, Acharya & BM Reddy College of Pharmacy, Bengaluru, Karnataka, India.ORCID https://orcid.org/0000-0002-4844-5776
Gurubasavaraja Swamy Purawarga MatadaDepartment of Pharmaceutical Chemistry, Integrated Drug Discovery Centre, Acharya & BM Reddy College of Pharmacy, Bengaluru, Karnataka, India. gurubasavarajaswamy@gmail.com.ORCID http://orcid.org/0000-0002-1978-6029
Dayananda Sagar University · INDr. Reddy's Laboratories (United States) · US

Funding

Indian Council of Medical Research 5/13/79/2020/NCD-III
6 · The paper itself

Abstract

BRAF is the most common serine-threonine protein kinase and regulates signal transduction from RAS to MEK inside the cell. The BRAF is a highly active isoform of RAF kinase. BRAF has two domains such as regulatory and kinase domains. The BRAF inhibitors bind in the c-terminus of the kinase domain and inhibit the downstream pathways. The mutation occurs mainly in the A-loop of the kinase domain. The mutation occurs due to a conversion of valine to glutamate/lysine/arginine/aspartic acid at 600th position. Among the diverse mutations, BRAF

Indexed as

Protein Kinase InhibitorsProto-Oncogene Proteins B-rafAnimalsAntineoplastic AgentsHumansMutationNeoplasmsSignal TransductionStructure-Activity RelationshipAntineoplastic AgentsBRAF protein, humanProtein Kinase InhibitorsProto-Oncogene Proteins B-rafBiological evaluationBRAF inhibitorsCancerDockingStructure–activity relationship

Identifiers

PMID37470921
OpenAlexW4384818626

What OpenQuestion holds

Textmetadata
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.