Evidence map›Paper›PMID 26871953›Full record

ArticlePloS one2016

Decreased TUSC3 Promotes Pancreatic Cancer Proliferation, Invasion and Metastasis.

Xiaoqiang Fan, Xiu Zhang, Jie Shen, Haibin Zhao, Xuetao Yu, Yong'an Chen, Zhuonan Zhuang, Xiaolong Deng, Hua Feng, Yunfei Wang and 1 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

19 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  11. TUSC3: functional duality of a cancer gene.Cellular and molecular life sciences : CMLS · 2018
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. TUSC3 suppresses glioblastoma development by inhibiting Akt signaling.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Article
  18. Review
  19. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Xiaoqiang FanDepartment of Oncology, Jimin Hospital, Shanghai, China.
Xiu ZhangDepartment of Oncology, Jimin Hospital, Shanghai, China.
Jie ShenDepartment of Oncology, Jimin Hospital, Shanghai, China.
Haibin ZhaoDepartment of Pathology, Taihu Hospital, Wuxi, Jiangsu Province, China.
Xuetao YuDepartment of Oncology, Jimin Hospital, Shanghai, China.
Yong'an ChenDepartment of Oncology, Jimin Hospital, Shanghai, China.
Zhuonan ZhuangDepartment of General Surgery, Shandong University Affiliated Qilu Hospital, Ji'nan, Shandong Province, China.
Xiaolong DengDepartment of Oncology, Jimin Hospital, Shanghai, China.
Hua FengDepartment of Oncology, Jimin Hospital, Shanghai, China.
Yunfei WangDepartment of Oncology, Jimin Hospital, Shanghai, China.
Long PengDepartment of Oncology, Jimin Hospital, Shanghai, China.
Qilu Hospital of Shandong University · CNWuxi Taihu Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is an aggressive disease with dismal prognosis. It is of paramount importance to understand the underlying etiological mechanisms and identify novel, consistent, and easy-to-apply prognostic factors for precision therapy. TUSC3 (tumor suppressor candidate 3) was identified as a potential tumor suppressor gene and previous study showed TUSC3 is decreased in pancreatic cancer at mRNA level, but its putative tumor suppressor function remains to be verified. In this study, TUSC3 expression was found to be suppressed both at mRNA and protein levels in cell line models as well as in clinical samples; decreased TUSC3 expression was associated with higher pathological TNM staging and poorer outcome. In three pairs of cell lines with different NF-κB activity, TUSC3 expression was found to be reversely correlated with NF-κB activity. TUSC3-silenced pancreatic cancer cell line exhibited enhanced potential of proliferation, migration and invasion. In an orthotopic implanted mice model, TUSC3 silenced cells exhibited more aggressive phenotype with more liver metastasis. In conclusion, the current study shows that decreased immunological TUSC3 staining is a factor prognostic of poor survival in pancreatic cancer patients and decreased TUSC3 promotes pancreatic cancer cell proliferation, invasion and metastasis. The reverse correlation between NF-κB activity and TUSC3 expression may suggest a novel regulation pattern for this molecule.

Indexed as

AdultAgedAnimalsBiomarkers, TumorCell Line, TumorCell ProliferationDisease-Free SurvivalFemaleGene ExpressionGene Knockdown TechniquesHumansLiver NeoplasmsLymphatic MetastasisMaleMembrane ProteinsMice, Inbred BALB CBiomarkers, TumorMembrane ProteinsNF-kappa BRNA, MessengerTumor Suppressor ProteinsTUSC3 protein, human

Identifiers

PMID26871953
PMCPMC4752499
OpenAlexW2256514090

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.