Evidence map›Paper›PMID 11313907›Full record

ReviewOncogene2001

G protein coupled receptor signaling through the Src and Stat3 pathway: role in proliferation and transformation.

P T Ram, R Iyengar

Abstract readReview
PubMed Publisher
In one paragraph

Review in Oncogene, 2001. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
3.3field-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

54 citing papers in PubMed, 136 citations in OpenAlex.

  1. Phase I Trial of TTI-101, a First-in-Class Oral Inhibitor of STAT3, in Patients with Advanced Solid Tumors.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
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  6. Review
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  19. Pharmacological Properties ofEC pharmacology and toxicology · 2019
    Article
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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

2 authors at 1 institution in 1 country.

P T RamDepartment of Pharmacology, Mount Sinai School of Medicine, New York, NY 10029, USA.
R Iyengar
Icahn School of Medicine at Mount Sinai · US

Funding

MOLECULAR MECHANISM OF DESENSITIZATIONR01GM054508 · NIGMS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI IYENGAR, SRINIVAS RAVI V · 1995 to 2016
$8.0M
SIGNALING PATHWAYS INTERACTIONS AND MAMMARY TUMORR01CA081050 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI IYENGAR, SRINIVAS RAVI V · 2000 to 2004
$1.8M
ADENYLYL CYCLASES IN TRANSFORMATION OF MAMMARY EPITHELIAF32CA079134 · NCI · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI RAM, PRAHLAD T · 1998 to 1999
–
NCI NIH HHS CA81050NCI NIH HHS F32 CA79134NIGMS NIH HHS GM54508
6 · The paper itself

Abstract

Extracellular signals when routed through signaling pathways that use heterotrimeric G proteins can engage multiple signaling pathways leading to diverse biological consequences. One locus at which signal sorting occurs is at the level of G proteins. G protein alpha-subunits appear to be capable of interacting with different effectors leading to engagement of distinct signaling pathways. Regulation of different pathways in turn leads to different biological outcomes. The process of neoplastic transformation is controlled to a large extent through the activation and inhibition of signaling pathways. Signaling pathways such as the Ras-MAPK, v-Src-Stat3 pathways are activated in the process of transformation. Expression of activated Galpha subunits have been shown to cause transformation of cells. While activation of the MAPK 1,2 pathway by various Galpha subunits has been reported for several years, recent studies show the activation and involvement of Src and Stat3 pathways in Galphao and Galphai mediated transformation of cells. Recent studies also suggest that both Galphai and Galphas may be able to interact with and activate Src. The activation of Src and Stat3 by G proteins has also been demonstrated by ligand-induced activation of G protein receptors. So increasingly it is becoming clear that the Src and Stat3 pathways are potential effectors for G proteins and that they may play a role in G protein function.

Indexed as

Cell Transformation, NeoplasticCell DivisionDNA-Binding ProteinsGTP-Binding ProteinsModels, BiologicalOncogene Protein pp60(v-src)Receptors, Cell SurfaceSignal TransductionSTAT3 Transcription FactorTrans-ActivatorsDNA-Binding ProteinsGTP-Binding ProteinsOncogene Protein pp60(v-src)Receptors, Cell SurfaceSTAT3 Transcription FactorTrans-Activators

Identifiers

PMID11313907
OpenAlexW1988656690

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.