Evidence map›Paper›PMID 30962722›Full record

ArticleCancer management and research2019

Linc01194 acts as an oncogene in colorectal carcinoma and is associated with poor survival outcome.

Xiaoxue Wang, Zhimin Liu, Hong Tong, Hui Peng, Zhenyu Xian, Li Li, Bang Hu, Shangkui Xie

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.1field-weighted citation impact, top 28% 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

10 citing papers in PubMed, 15 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 1 country.

Xiaoxue WangDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Zhimin LiuDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Hong TongDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Hui PengDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Zhenyu XianDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Li LiDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Bang HuDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Shangkui XieDepartment of Proctology, The Sixth Affiliated Hospital of Sun Yat-Sen University, Guangzhou, People's Republic of China, shangkuixie12@126.com.
Sixth Affiliated Hospital of Sun Yat-sen University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe incidence of colorectal cancer ranks among the top three malignant tumors, attributing to more than 50,000 deaths in the United States every year. Survival rate is directly correlated with TNM stage at diagnosis, and identifying the molecules involved in the cancer development process will provide directions to better investigate the mechanisms of colorectal cancer. MATERIALS AND

methodsBioinformatics analysis of differentially expressed long noncoding RNAs (lncRNAs), survival analysis, cell proliferation assay, migration assay, and Western blot analysis were performed.

resultsFifty-one lncRNAs were identified between the early stage and late-stage groups. In the survival analysis, we found that Linc01194 is correlated with poor survival of colon cancer patients. In addition, by suppressing the expression of Linc01194 in colon cancer cell lines, cell proliferation and migration were inhibited. Western blot showed that N-cadherin and vimentin were downregulated, whereas E-cadherin was upregulated indicating that the process of epithelial-mesenchymal transition (EMT) was restrained.

conclusion

Indexed as

colorectal cancerEMTLinc01194lncRNATCGA

Identifiers

PMID30962722
PMCPMC6434913
OpenAlexW2924407454

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.