Evidence map›Paper›PMID 27012470›Full record

ArticleInternational journal of cancer2016

Suppression of pancreatic cancer growth and metastasis by HMP19 identified through genome-wide shRNA screen.

Hiroshi Kurahara, Christopher Bohl, Shoji Natsugoe, Yuka Nishizono, Sitaram Harihar, Rahul Sharma, Tomoo Iwakuma, Danny R Welch

Open access · hybridAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

8 authors at 2 institutions in 2 countries.

Hiroshi KuraharaDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS.
Christopher BohlDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS.
Shoji NatsugoeDepartment of Digestive Surgery, Breast and Thyroid Surgery, Kagoshima University, Kagoshima, Japan.
Yuka NishizonoDepartment of Digestive Surgery, Breast and Thyroid Surgery, Kagoshima University, Kagoshima, Japan.
Sitaram HariharDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS.
Rahul SharmaDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS.
Tomoo IwakumaDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS.
Danny R WelchDepartment of Cancer Biology, University of Kansas Medical Center, Kansas City, KS.ORCID 0000-0002-1951-4947
The University of Kansas Cancer Center · USKagoshima University · JP

Funding

Transgenic & Gene-Targeting Shared ResourceP30CA168524 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI NICOLE L NOLLEN · 2012 to 2026
$40.1M
The role of MDM2-MTBP axis in cancer metastasisR01CA174735 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI IWAKUMA, TOMOO · 2014 to 2018
$1.6M
KISS1: Defining Mechanisms for Antimetastatic TherapyR01CA134981 · NCI · UNIVERSITY OF KANSAS MEDICAL CENTER · PI WELCH, DANNY R. · 2009 to 2014
$1.5M
NCI NIH HHS P30 CA168524NCI NIH HHS R01 CA134981NCI NIH HHS R01 CA174735
6 · The paper itself

Abstract

Therapeutic effectiveness against metastatic or even locally advanced pancreatic ductal adenocarcinoma (PDAC) is dismal, with 5-year survival less than 5%. Even in patients who undergo potentially curative resection, most patients' tumors recur in the liver. Improving therapies targeting or preventing liver metastases is crucial for improving prognosis. To identify genes suppressing metastasis, a genome-wide shRNA screen was done using the human non-metastatic PDAC cell line, S2-028. After identification of candidates, functional validation was done using intrasplenic and orthotopic injections in athymic mice. HMP19 strongly inhibited metastasis but also partially attenuated tumor growth in the pancreas. Knockdown of HMP19 increased localization of activated ERK1/2 in the nucleus, corresponding to facilitated cell proliferation, decreased p27(Kip1) and increased cyclin E1. Over-expression of HMP19 exerted the opposite effects. Using a tissue microarray of 84 human PDAC, patients with low expression of HMP19 showed significantly higher incidence of liver metastasis (p = 0.0175) and worse prognosis (p = 0.018) after surgery. HMP19, a new metastasis/tumor suppressor in PDAC, appears to alter signaling that leads to cell proliferation and appears to offer prognostic value in human PDAC.

Indexed as

Genome-Wide Association StudyAnimalsCell Line, TumorCell MovementCell ProliferationDisease Models, AnimalGene Knockdown TechniquesHumansLiver NeoplasmsMiceMice, NudeNeoplasm MetastasisPancreatic NeoplasmsRNA, Small InterferingTumor BurdenRNA, Small Interferingcell cyclecyclin EERKmetastasismetastasis suppressorp27kip1pancreatic ductal adenocarcinomashRNA

Identifiers

PMID27012470
PMCPMC4867126
OpenAlexW2307909711

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.