Evidence map›Paper›PMID 33763427›Full record

ArticleFrontiers in cell and developmental biology2021

LMO7 as an Unrecognized Factor Promoting Pancreatic Cancer Progression and Metastasis.

Xinjian Liu, Hao Yuan, Jing Zhou, Qiongling Wang, Xiaoqiang Qi, Catharine Bernal, Diego Avella, Jussuf T Kaifi, Eric T Kimchi, Parrett Timothy and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cell and developmental biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 18% 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

22 citing papers in PubMed, 26 citations in OpenAlex.

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  12. Role of LMO7 in cancer (Review).Oncology reports · 2024
    Review
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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

14 authors at 4 institutions in 2 countries.

Xinjian LiuDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Hao YuanDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Jing ZhouDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Qiongling WangDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Xiaoqiang QiDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Catharine BernalDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Diego AvellaDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Jussuf T KaifiDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Eric T KimchiDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Parrett TimothyDepartment of Pathology and Anatomical Sciences, University of Missouri-Columbia, Columbia, MO, United States.
Kun ChengDivision of Pharmacology and Pharmaceutical Sciences, School of Pharmacy, University of Missouri-Kansas City, Kansas City, MO, United States.
Yi MiaoPancreas Center, The First Affiliated Hospital of Nanjing Medical University, Nanjing, China.
Kuirong JiangDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
Guangfu LiDepartment of Surgery, University of Missouri-Columbia, Columbia, MO, United States.
University of Missouri · USNanjing Medical University · CNJiangsu Province Hospital · CNUniversity of Missouri–Kansas City · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer (PC) is one of the most lethal human malignancies without effective treatment. In an effort to discover key genes and molecular pathways underlying PC growth, we have identified LIM domain only 7 (LMO7) as an under-investigated molecule, which highly expresses in primary and metastatic human and mouse PC with the potential of impacting PC tumorigenesis and metastasis. Using genetic methods with siRNA, shRNA, and CRISPR-Cas9, we have successfully generated stable mouse PC cells with LMO7 knockdown or knockout. Using these cells with loss of LMO7 function, we have demonstrated that intrinsic LMO7 defect significantly suppresses PC cell proliferation, anchorage-free colony formation, and mobility

Indexed as

apoptosiscell cycleCRISPR-Cas9LIM domain only 7 (LMO7)pancreatic cancer

Identifiers

PMID33763427
PMCPMC7982467
OpenAlexW3133491070

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.