Evidence map›Paper›PMID 22952058›Full record

ArticleMolecular medicine (Cambridge, Mass.)2012

CSE1L, a novel microvesicle membrane protein, mediates Ras-triggered microvesicle generation and metastasis of tumor cells.

Ching-Fong Liao, Shu-Hui Lin, Hung-Chang Chen, Cheng-Jeng Tai, Chun-Chao Chang, Li-Tzu Li, Chung-Min Yeh, Kun-Tu Yeh, Ying-Chun Chen, Tsu-Han Hsu and 5 more

Open access · goldAbstract read
In one paragraph

Article in Molecular medicine (Cambridge, Mass.), 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

36 citing papers in PubMed, 63 citations in OpenAlex.

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  4. Mechanism of exportin retention in the cell nucleus.The Journal of cell biology · 2024
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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

15 authors at 8 institutions in 1 country.

Ching-Fong LiaoInstitute of Cellular and Organismic Biology, Academia Sinica, Taipei, Taiwan.
Shu-Hui Lin
Hung-Chang Chen
Cheng-Jeng Tai
Chun-Chao Chang
Li-Tzu Li
Chung-Min Yeh
Kun-Tu Yeh
Ying-Chun Chen
Tsu-Han Hsu
Shing-Chuan Shen
Woan-Ruoh Lee
Jeng-Fong Chiou
Shue-Fen Luo
Ming-Chung Jiang
Academia Sinica · TWTaipei Medical University · TWTaipei Medical University Hospital · TWChanghua Christian Hospital · TWChang Gung Memorial Hospital · TWInstitute of Cellular and Organismic Biology, Academia Sinica · TWKang-Ning Junior College of Medical Care and Management · TWKaohsiung Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor-derived microvesicles are rich in metastasis-related proteases and play a role in the interactions between tumor cells and tumor microenvironment in tumor metastasis. Because shed microvesicles may remain in the extracellular environment around tumor cells, the microvesicle membrane protein may be the potential target for cancer therapy. Here we report that chromosome segregation 1-like (CSE1L) protein is a microvesicle membrane protein and is a potential target for cancer therapy. v-H-Ras expression induced extracellular signal-regulated kinase (ERK)-dependent CSE1L phosphorylation and microvesicle biogenesis in various cancer cells. CSE1L overexpression also triggered microvesicle generation, and CSE1L knockdown diminished v-H-Ras-induced microvesicle generation, matrix metalloproteinase (MMP)-2 and MMP-9 secretion and metastasis of B16F10 melanoma cells. CSE1L was preferentially accumulated in microvesicles and was located in the microvesicle membrane. Furthermore, anti-CSE1L antibody-conjugated quantum dots could target tumors in animal models. Our findings highlight a novel role of Ras-ERK signaling in tumor progression and suggest that CSE1L may be involved in the "early" and "late" metastasis of tumor cells in tumorigenesis. Furthermore, the novel microvesicle membrane protein, CSE1L, may have clinical utility in cancer diagnosis and targeted cancer therapy.

Indexed as

AnimalsAntibodiesCell-Derived MicroparticlesCell Line, TumorCellular Apoptosis Susceptibility ProteinExtracellular Signal-Regulated MAP KinasesHumansMaleMiceMice, Inbred C57BLNeoplasm MetastasisNeoplasmsPhosphorylationPhosphothreonineras ProteinsAntibodiesCellular Apoptosis Susceptibility ProteinExtracellular Signal-Regulated MAP KinasesPhosphothreonineras Proteins

Identifiers

PMID22952058
PMCPMC3521793
OpenAlexW1578834667

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.