Evidence map›Paper›PMID 26934315›Full record

ArticleOncotarget2016

PARP6 acts as a tumor suppressor via downregulating Survivin expression in colorectal cancer.

Guangying Qi, Yasusei Kudo, Bo Tang, Tian Liu, Shengjian Jin, Jing Liu, Xiaoxu Zuo, Sisi Mi, Wenhuan Shao, Xiaojuan Ma and 5 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 32 citations in OpenAlex.

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  10. Research Progress on Mono-ADP-Ribosyltransferases in Human Cell Biology.Frontiers in cell and developmental biology · 2022
    Review
  11. Article
  12. Functional roles of ADP-ribosylation writers, readers and erasers.Frontiers in cell and developmental biology · 2022
    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

15 authors at 3 institutions in 2 countries.

Guangying QiDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Yasusei KudoDepartment of Oral Molecular Pathology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8504, Japan.
Bo TangDepartment of Hepatobiliary Surgery, Affiliated Hospital of Guilin Medical University, Guilin 541000, People's Republic of China.
Tian LiuDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Shengjian JinDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Jing LiuDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Xiaoxu ZuoDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Sisi MiDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Wenhuan ShaoDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Xiaojuan MaDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Takaaki TsunematsuDepartment of Oral Molecular Pathology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8504, Japan.
Naozumi IshimaruDepartment of Oral Molecular Pathology, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima 770-8504, Japan.
Sien ZengDepartment of Pathology and Physiopathology, Guilin Medical University, Guilin 541004, People's Republic of China.
Masaaki TatsukaDepartment of Life Sciences, Faculty of Life and Environmental Sciences, Prefectural University of Hiroshima, Hiroshima 727-0023, Japan.
Fumio ShimamotoDepartment of Health Sciences, Prefectural University of Hiroshima, Hiroshima 734-8558, Japan.
Guilin Medical University · CNPrefectural University of Hiroshima · JPTokushima University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poly (ADP-ribose) polymerases (PARPs) are enzymes that transfer ADP-ribose groups to target proteins and are involved in a variety of biological processes. PARP6 is a novel member, and our previous findings suggest that PARP6 may act as a tumor suppressor via suppressing cell cycle progression. However, it is still unclear that PARP6 function besides growth suppression in colorectal cancer (CRC). In this study, we examined tumor suppressive roles of PAPR6 in CRC cells both in vitro and in vivo. We found that PARP6 inhibited colony formation, invasion and migration as well as cell proliferation. Moreover, ectopic overexpression of PARP6 decreased Survivin expression, which acts as an oncogene and is involved in apoptosis and mitosis. We confirmed the inverse correlation between PARP6 and Survivin expression in CRC cases by immunohistochemistry. Importantly, CRC cases with downregulation of PARP6 and upregulation of Survivin showed poor prognosis. In summary, PARP6 acts as a tumor suppressor via downregulating Survivin expression in CRC. PARP6 can be a novel diagnostic and therapeutic target together with Survivin for CRC.

Indexed as

ADP Ribose TransferasesCell ProliferationColorectal NeoplasmsDown-RegulationFemaleGenes, Tumor SuppressorHumansInhibitor of Apoptosis ProteinsMaleSignal TransductionSurvivinADP Ribose TransferasesBIRC5 protein, humanInhibitor of Apoptosis ProteinsPARP6 protein, humanSurvivincolorectal cancerPARP6prognosisSurvivintumor suppressor

Identifiers

PMID26934315
PMCPMC4951331
OpenAlexW2295626371

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.