Evidence map›Paper›PMID 29108261›Full record

ArticleOncotarget2017

The coiled-coil domain of oncogene RASSF 7 inhibits hippo signaling and promotes non-small cell lung cancer.

Xiaoying Zheng, Qianze Dong, Xiupeng Zhang, Qiang Han, Xu Han, Yong Han, Jingjing Wu, Xuezhu Rong, Enhua Wang

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.8field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. A Number of the N-terminal RASSF Family: RASSF7.Anti-cancer agents in medicinal chemistry · 2024
    Pooled it
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  5. Observational
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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 1 institution in 1 country.

Xiaoying ZhengDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Qianze DongDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Xiupeng ZhangDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Qiang HanDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Xu HanDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Yong HanDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Jingjing WuDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Xuezhu RongDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
Enhua WangDepartment of Pathology, College of Basic Medical Science and First Affiliated Hospital, China Medical University, Shenyang, China.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer is the leading cause of cancer-related deaths worldwide, and despite recent improvements in treatment patient prognosis remains dismal. In this study, we examined the role of N-terminal Ras-association domain family 7 (RASSF7) in human non-small cell lung cancer (NSCLC). We found that RASSF7 was overexpressed NSCLC tissues, which correlated with advanced TNM stage, positive lymph node metastasis, and poor prognosis. This RASSF7 overexpression promoted lung cancer cell proliferation, migration, and invasion. We also found that RASSF7 interacted with mammalian Ste20-like kinase 1(MST1) through its C-terminal coiled-coil domain to inhibit MST1 phosphorylation as well as the phosphorylation of large tumor suppressor kinase 1(LATS1) and yes-associated protein (YAP), while promoting the nuclear translocation of YAP. In addition, RASSF7 overexpression inhibited the Hippo signaling pathway both in

Indexed as

hippo signaling pathwaymigrationnon-small cell lung cancerproliferationRASSF7

Identifiers

PMID29108261
PMCPMC5667994
OpenAlexW2742286087

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.