Evidence map›Paper›PMID 26804173›Full record

ArticleOncogene2016

Therapeutic targeting of tetraspanin8 in epithelial ovarian cancer invasion and metastasis.

C S Park, T-K Kim, H G Kim, Y-J Kim, M H Jeoung, W R Lee, N K Go, K Heo, S Lee

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
6.0field-weighted citation impact, top 3% 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

47 citing papers in PubMed, 65 citations in OpenAlex.

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  4. Single-Cell RNA Sequencing of Ewing Sarcoma Tumors Demonstrates Transcriptional Heterogeneity and Clonal Evolution.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
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  19. Assessment of TSPAN Expression Profile and Their Role in the VSCC Prognosis.International journal of molecular sciences · 2021
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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

9 authors at 2 institutions in 1 country.

C S ParkLaboratory of Molecular Cancer Therapeutics, Scripps Korea Antibody Institute,, Chuncheon-si, Korea.
T-K KimLaboratory of Molecular Cancer Therapeutics, Scripps Korea Antibody Institute,, Chuncheon-si, Korea.
H G KimNew Experimental Therapeutics Branch, Research Institute, National Cancer Center, Goyang-si, Korea.
Y-J KimSpecific Organs Cancer Branch, Research Institute, National Cancer Center, Goyang-si, Korea.
M H JeoungLaboratory of Molecular Cancer Therapeutics, Scripps Korea Antibody Institute,, Chuncheon-si, Korea.
W R LeeLaboratory of Molecular Cancer Therapeutics, Scripps Korea Antibody Institute,, Chuncheon-si, Korea.
N K GoLaboratory of Molecular Cancer Therapeutics, Scripps Korea Antibody Institute,, Chuncheon-si, Korea.
K HeoNew Experimental Therapeutics Branch, Research Institute, National Cancer Center, Goyang-si, Korea.
S LeeLaboratory of Molecular Cancer Therapeutics, Scripps Korea Antibody Institute,, Chuncheon-si, Korea.
Scripps Korea Antibody Institute · KRNational Cancer Center · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epithelial ovarian cancer (EOC) invasion and metastasis are complex phenomena that result from the coordinated action of many metastatic regulators and must be overcome to improve clinical outcomes for patients with these cancers. The identification of novel therapeutic targets is critical because of the limited success of current treatment regimens, particularly in advanced-stage ovarian cancers. In this study, we found that tetraspanin 8 (TSPAN8) is overexpressed in about 52% (14/27) of EOC tissues and correlates with poor survival. Using small interfering RNA-mediated TSPAN8 knockdown and a competition assay with purified TSPAN8 large extracellular loop (TSPAN8-LEL) protein, we identified TSPAN8-LEL as a key regulator of EOC cell invasion. Furthermore, monotherapy with TSPAN8-blocking antibody we developed shows that antibody-based modulation of TSPAN8-LEL can significantly reduce the incidence of EOC metastasis without severe toxicity in vivo. Finally, we demonstrated that the TSPAN8-blocking antibody promotes the internalization and concomitant downregulation of cell surface TSPAN8. Collectively, our data suggest TSPAN8 as a potential novel therapeutic target in EOCs and antibody targeting of TSPAN8 as an effective strategy for inhibiting invasion and metastasis of TSPAN8-expressing EOCs.

Indexed as

AntibodiesCarcinoma, Ovarian EpithelialFemaleHumansImmunoglobulin GNeoplasm InvasivenessNeoplasm MetastasisNeoplasms, Glandular and EpithelialOvarian NeoplasmsTetraspaninsAntibodiesImmunoglobulin GTetraspaninsTSPAN8 protein, human

Identifiers

PMID26804173
OpenAlexW2265677187

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.