Evidence map›Paper›PMID 24704825›Full record

ArticleOncogene2015

LNK (SH2B3): paradoxical effects in ovarian cancer.

L-W Ding, Q-Y Sun, D-C Lin, W Chien, N Hattori, X-M Dong, S Gery, M Garg, N B Doan, J W Said and 7 more

Abstract read
In one paragraph

Article in Oncogene, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Lnk Governs chemokine-directed trafficking of CD8Molecular therapy. Oncology · 2026
    Article
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  10. The multifaceted role of reactive oxygen species in tumorigenesis.Cellular and molecular life sciences : CMLS · 2020
    Review
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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

17 authors at 6 institutions in 2 countries.

L-W DingCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
Q-Y SunCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
D-C Lin1] Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore [2] Division of Hematology/Oncology, Cedar-Sinai Medical Center, UCLA School of Medicine, Los Angeles, CA, USA.
W ChienCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
N HattoriCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
X-M DongSchool of Biology Science, Nanyang Technological University, Singapore, Singapore.
S GeryDivision of Hematology/Oncology, Cedar-Sinai Medical Center, UCLA School of Medicine, Los Angeles, CA, USA.
M GargCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
N B DoanSanta Monica-University of California, Los Angeles Medical Center, Los Angeles, CA, USA.
J W SaidSanta Monica-University of California, Los Angeles Medical Center, Los Angeles, CA, USA.
J-F XiaoCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
H YangCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
L-Z LiuCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
X MengCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
R Y-J HuangCancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore.
K TangSchool of Biology Science, Nanyang Technological University, Singapore, Singapore.
H P Koeffler1] Cancer Science Institute of Singapore, National University of Singapore, Singapore, Singapore [2] Division of Hematology/Oncology, Cedar-Sinai Medical Center, UCLA School of Medicine, Los Angeles, CA, USA [3] National University Cancer Institute, National University Hospital Singapore, Singapore, Singapore.
National University of Singapore · SGNational University Cancer Institute, Singapore · SGCedars-Sinai Medical Center · USNanyang Technological University · SGLos Angeles Medical Center · USUniversity of California, Los Angeles · US

Funding

REGULATION OF HEMATOPOIETIC CYTOKINESR01CA026038 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KOEFFLER, HAROLD PHILLIP · 1985 to 2013
$4.7M
NCI NIH HHS R01 CA026038NCI NIH HHS R01CA026038-33
6 · The paper itself

Abstract

LNK (SH2B3) is an adaptor protein studied extensively in normal and malignant hematopoietic cells. In these cells, it downregulates activated tyrosine kinases at the cell surface resulting in an antiproliferative effect. To date, no studies have examined activities of LNK in solid tumors. In this study, we found by in silico analysis and staining tissue arrays that the levels of LNK expression were elevated in high-grade ovarian cancer. To test the functional importance of this observation, LNK was either overexpressed or silenced in several ovarian cancer cell lines. Remarkably, overexpression of LNK rendered the cells resistant to death induced by either serum starvation or nutrient deprivation, and generated larger tumors using a murine xenograft model. In contrast, silencing of LNK decreased ovarian cancer cell growth in vitro and in vivo. Western blot studies indicated that overexpression of LNK upregulated and extended the transduction of the mitogenic signal, whereas silencing of LNK produced the opposite effects. Furthermore, forced expression of LNK reduced cell size, inhibited cell migration and markedly enhanced cell adhesion. Liquid chromatography-mass spectroscopy identified 14-3-3 as one of the LNK-binding partners. Our results suggest that in contrast to the findings in hematologic malignancies, the adaptor protein LNK acts as a positive signal transduction modulator in ovarian cancers.

Indexed as

14-3-3 ProteinsAdaptor Proteins, Signal TransducingAnimalsCell AdhesionCell Line, TumorCell MovementCell ProliferationCell SizeFemaleHumansIntracellular Signaling Peptides and ProteinsMiceMice, Inbred NODMice, SCIDMitogen-Activated Protein KinasesNeoplasm Transplantation14-3-3 ProteinsAdaptor Proteins, Signal TransducingIntracellular Signaling Peptides and ProteinsMitogen-Activated Protein KinasesProteinsProto-Oncogene Proteins c-aktSH2B3 protein, humanYWHAB protein, human

Identifiers

PMID24704825
PMCPMC4188804
OpenAlexW2011637263

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.