Evidence map›Paper›PMID 29455658›Full record

ReviewMolecular cancer2018

Receptor tyrosine kinases (RTKs) in breast cancer: signaling, therapeutic implications and challenges.

Ramesh Butti, Sumit Das, Vinoth Prasanna Gunasekaran, Amit Singh Yadav, Dhiraj Kumar, Gopal C Kundu

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06494865 (" Role of Diffusion Weighted Image in the Diagnosis and Follow up of Breast Cancer"), which is not on this map. Cited by 190 papers.

0numbers the graph read from it
0cells of the map it votes in
190citing papers in PubMed
10.9field-weighted citation impact, top 1% 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.

NCT06494865 not yet recruitingnot on this mapstarted 2024, after this paper: background citation

" Role of Diffusion Weighted Image in the Diagnosis and Follow up of Breast Cancer"

TypeobservationalSponsorSohag UniversityRan2024 to 2024Enrolled30ConditionsBreast CancerArmsMRI device
3 · Its place in the literature

Who cites it

190 citing papers in PubMed, 395 citations in OpenAlex.

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130 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 2 countries.

Ramesh ButtiLaboratory of Tumor Biology, Angiogenesis and Nanomedicine Research, National Centre for Cell Science, SP Pune University Campus, Pune, 411007, India.
Sumit DasLaboratory of Tumor Biology, Angiogenesis and Nanomedicine Research, National Centre for Cell Science, SP Pune University Campus, Pune, 411007, India.
Vinoth Prasanna GunasekaranLaboratory of Tumor Biology, Angiogenesis and Nanomedicine Research, National Centre for Cell Science, SP Pune University Campus, Pune, 411007, India.
Amit Singh YadavLaboratory of Tumor Biology, Angiogenesis and Nanomedicine Research, National Centre for Cell Science, SP Pune University Campus, Pune, 411007, India.
Dhiraj KumarDepartment of Cancer Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, 77054, USA.
Gopal C KunduLaboratory of Tumor Biology, Angiogenesis and Nanomedicine Research, National Centre for Cell Science, SP Pune University Campus, Pune, 411007, India. kundu@nccs.res.in.
National Centre for Cell Science · INThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is a multifactorial disease and driven by aberrant regulation of cell signaling pathways due to the acquisition of genetic and epigenetic changes. An array of growth factors and their receptors is involved in cancer development and metastasis. Receptor Tyrosine Kinases (RTKs) constitute a class of receptors that play important role in cancer progression. RTKs are cell surface receptors with specialized structural and biological features which respond to environmental cues by initiating appropriate signaling cascades in tumor cells. RTKs are known to regulate various downstream signaling pathways such as MAPK, PI3K/Akt and JAK/STAT. These pathways have a pivotal role in the regulation of cancer stemness, angiogenesis and metastasis. These pathways are also imperative for a reciprocal interaction of tumor and stromal cells. Multi-faceted role of RTKs renders them amenable to therapy in breast cancer. However, structural mutations, gene amplification and alternate pathway activation pose challenges to anti-RTK therapy.

Indexed as

Antineoplastic AgentsBreast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor Protein-Tyrosine KinasesSignal TransductionAntineoplastic AgentsPhosphatidylinositol 3-KinasesProto-Oncogene Proteins c-aktReceptor Protein-Tyrosine KinasesAlternate pathway activationAngiogenesisAnti-RTK therapyBevacizumabBrest cancerCancer Stem cellsDrug resistanceLapatinibMetastasisTrastuzumabTumor microenvironmentTumor-stroma interaction

Identifiers

PMID29455658
PMCPMC5817867
OpenAlexW2795063553

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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 Socratic graph.