Evidence map›Paper›PMID 24695631›Full record

ArticleInternational journal of clinical and experimental pathology2014

Lemur tyrosine kinase-3 is a significant prognostic marker for patients with colorectal cancer.

Hongbing Shi, Qing Li, Mei Ji, Jun Wu, Zhengguang Li, Xiao Zheng, Bin Xu, Lujun Chen, Xiaodong Li, Changqing Lu and 3 more

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.1field-weighted citation impact, top 48% 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

14 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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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

13 authors at 1 institution in 2 countries.

Hongbing ShiDepartment of Oncology, The Third Affiliated Hospital of Soochow University Soochow, China.
Qing LiDepartment of Pathology, The Third Affiliated Hospital of Soochow University Soochow, China.
Mei JiDepartment of Oncology, The Third Affiliated Hospital of Soochow University Soochow, China.
Jun WuDepartment of Oncology, The Third Affiliated Hospital of Soochow University Soochow, China.
Zhengguang LiDepartment of Oncology, The Third Affiliated Hospital of Soochow University Soochow, China.
Xiao ZhengDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University Soochow, China.
Bin XuDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University Soochow, China.
Lujun ChenDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University Soochow, China.
Xiaodong LiDepartment of Oncology, The Third Affiliated Hospital of Soochow University Soochow, China.
Changqing LuDepartment of Pathology, The Third Affiliated Hospital of Soochow University Soochow, China.
Yan TanDepartment of Pathology, The Third Affiliated Hospital of Soochow University Soochow, China.
Changping WuDepartment of Oncology, The Third Affiliated Hospital of Soochow University Soochow, China.
Jingting JiangDepartment of Tumor Biological Treatment, The Third Affiliated Hospital of Soochow University Soochow, China.
Soochow University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lemur tyrosine kinase-3 (LMTK3) belongs to the family of serine-threonine-tyrosine kinases and the aberrant expression of LMTK3 was observed in several human malignancies. However, the association of LMTK3 with clinical outcomes in colorectal cancer patients is unclear. Thus, this present study was to evaluate the association of LMTK3 expression level with clinicopathologic factors and prognosis of patients with colorectal cancer (CRC). The expression level of LMTK3 in 69 archival paraffin-embedded colorectal tumor tissue specimens was examined by immunohistochemistry (IHC). As a result, we found that the LMTK3 expression level was significantly elevated in CRC tissues as compared with Crohn's disease or colorectal polyp tissues (P<0.0001, P<0.0001, respectively). Positive LMTK3 signals in the colorectal cancer cells were observed in about 89.9% (62 of 69) CRC tissue specimens. Additionally, LMTK3 expression was significantly correlated with lymph node metastasis and tumor-node-metastasis (TNM) classification (P=0.003, and P=0.008, respectively), but not with sex, age, tumor location, histological differentiation, tumor size, or depth of tumor invasion (all P>0.05). Kaplan-Meier survival curves showed that the overall survival rate was significantly higher in the patients with low expression of LMTK3 when compared with those patients with high LMTK3 (P=0.010). Moreover, multivariate analysis revealed that LMTK3 expression was an independent prognostic factor for CRC patients (P=0.047). These results suggest that LMTK3 protein could serve as a prognostic marker for CRC patients.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorColorectal NeoplasmsFemaleHumansImmunohistochemistryKaplan-Meier EstimateMaleMembrane ProteinsMiddle AgedPrognosisProportional Hazards ModelsProtein Serine-Threonine KinasesBiomarkers, TumorLMTK3 protein, humanMembrane ProteinsProtein Serine-Threonine KinasesColorectal cancerimmunohistochemistry (ihc)lemur tyrosine kinase-3 (lmtk3)prognosis

Identifiers

PMID24695631
PMCPMC3971314
OpenAlexW19122584

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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.