Evidence map›Paper›PMID 25525286›Full record

ArticleDisease markers2014

High SHIP2 expression indicates poor survival in colorectal cancer.

Ju Yang, Maoying Fu, Yaoguang Ding, Yajing Weng, Weifei Fan, Xiaolin Pu, Zhijun Ge, Feng Zhan, Huihui Ni, Wei Zhang and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Disease markers, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

18 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
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  13. INPPL1 gene mutations in opsismodysplasia.Journal of human genetics · 2017
    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

16 authors at 6 institutions in 1 country.

Ju YangDepartment of Gastroenterology, Kunshan Hospital of Traditional Chinese Medicine, The Affiliated Hospital of Nanjing University of Chinese Medicine, Suzhou 215000, China.
Maoying FuDepartment of Infectious Diseases, The First People's Hospital of Kunshan Affiliated with Jiangsu University, Suzhou 215000, China.
Yaoguang DingDepartment of Oncology, Kunshan Hospital of Traditional Chinese Medicine, The Affiliated Hospital of Nanjing University of Chinese Medicine, Suzhou 215000, China.
Yajing WengDepartment of Geriatric Rehabilitation, Kunshan Hospital of Traditional Chinese Medicine, The Affiliated Hospital of Nanjing University of Chinese Medicine, Suzhou 215000, China.
Weifei FanDepartment of Hematology and Oncology, Jiangsu Province Geriatric Institute, Nanjing 210000, China.
Xiaolin PuDepartment of Hematology and Oncology, Jiangsu Province Geriatric Institute, Nanjing 210000, China.
Zhijun GeDepartment of Anesthesiology, Yixing People's Hospital, The Affiliated Yixing Hospital of Jiangsu University, Yixing 214200, China.
Feng ZhanDepartment of Hepatobiliary and Laparoscopic Surgery, Yixing People's Hospital, The Affiliated Yixing Hospital of Jiangsu University, Yixing 214200, China.
Huihui NiDepartment of Infectious Diseases, The First People's Hospital of Kunshan Affiliated with Jiangsu University, Suzhou 215000, China.
Wei ZhangDepartment of Infectious Diseases, The First People's Hospital of Kunshan Affiliated with Jiangsu University, Suzhou 215000, China.
Feng JinDepartment of Infectious Diseases, The First People's Hospital of Kunshan Affiliated with Jiangsu University, Suzhou 215000, China.
Ning XuDepartment of Pathology, Nanjing Medical University, Nanjing 210000, China.
Jiang LiDepartment of Pathology, Jiangsu Province Geriatric Institute, Nanjing 210000, China.
Liang QiuDepartment of Pathology, Jiangsu Province Geriatric Institute, Nanjing 210000, China.
Jun WangDepartment of Hematology and Oncology, Jiangsu Province Geriatric Institute, Nanjing 210000, China.
Xuefeng GuDepartment of Infectious Diseases, The First People's Hospital of Kunshan Affiliated with Jiangsu University, Suzhou 215000, China.
First People's Hospital of Kunshan · CNJiangsu University · CNNanjing University of Chinese Medicine · CNYixing People's Hospital · CNNanjing Medical University · CNShanghai University of Traditional Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

SH2-containing inositol 5'-phosphatase 2 (SHIP2), which generally regulates insulin signaling, cytoskeleton remodeling, and receptor endocytosis, has been suggested to play a significant role in tumor development and progression. However, the associations between SHIP2 expression and the clinical features to evaluate its clinicopathologic significance in colorectal cancer (CRC) have not been determined yet. In the present study, one-step quantitative real-time polymerase chain reaction (qPCR) test and immunohistochemistry (IHC) analysis with CRC tissue microarrays (TMA) were employed to evaluate the mRNA and protein expression of SHIP2 in CRC. The results showed that SHIP2 expression in the mRNA and protein levels was significantly higher in CRC tissues than that in corresponding noncancerous tissues (both P < 0.05). The expression of SHIP2 protein in CRC was related to lymph node metastasis (P = 0.036), distant metastasis (P = 0.001), and overall survival (P = 0.009). Kaplan-Meier method and Cox multifactor analysis suggested that high SHIP2 protein level (P = 0.040) and positive distant metastasis (P = 0.048) were critically associated with the unfavorable survival of CRC patients. The findings suggested that SHIP2 may be identified as a useful prognostic marker in CRC and targeting CRC may provide novel strategy for CRC treatment.

Indexed as

AdenocarcinomaAgedBiomarkers, TumorColorectal NeoplasmsFemaleGene ExpressionHumansKaplan-Meier EstimateLymphatic MetastasisMaleMiddle AgedMultivariate AnalysisPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphoric Monoester HydrolasesProportional Hazards ModelsBiomarkers, TumorINPPL1 protein, humanPhosphatidylinositol-3,4,5-Trisphosphate 5-PhosphatasesPhosphoric Monoester Hydrolases

Identifiers

PMID25525286
PMCPMC4265379
OpenAlexW2134989568

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.