Evidence map›Paper›PMID 26101709›Full record

ArticleAmerican journal of cancer research2015

SP1-mediated microRNA-520d-5p suppresses tumor growth and metastasis in colorectal cancer by targeting CTHRC1.

Li Yan, Jiang Yu, Fei Tan, Geng-Tai Ye, Zhi-Yong Shen, Hao Liu, Yan Zhang, Jie-Fu Wang, Xian-Jun Zhu, Guo-Xin Li

Open access · greenAbstract read
In one paragraph

Article in American journal of cancer research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 49 citations in OpenAlex.

  1. Article
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  4. Review
  5. Review
  6. Biological factors driving colorectal cancer metastasis.World journal of gastrointestinal oncology · 2024
    Review
  7. Endothelin-3 is epigenetically silenced in endometrioid endometrial cancer.Journal of cancer research and clinical oncology · 2023
    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

10 authors at 2 institutions in 2 countries.

Li YanDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Jiang YuDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Fei TanDepartment of Minimally Invasive Gastrointestinal Surgery, Beijing Cancer Hospital and Institute, Peking University Cancer Hospital, Peking University School of Oncology, Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education) Beijing 100142, China.
Geng-Tai YeDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Zhi-Yong ShenDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Hao LiuDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Yan ZhangDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Jie-Fu WangDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Xian-Jun ZhuDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Guo-Xin LiDepartment of General Surgery, Nanfang Hospital, Southern Medical University No.1838 Guangzhou Avenue North, Guangzhou 510515, Guangdong, China.
Nanfang Hospital · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent evidence suggests that miR-520 family has an important role in regulating tumorigenesis and development of various types of solid cancers. However, as one of the most common cancers in the world, there is little known about the underlying regulatory mechanisms of miR-520 in colorectal cancer (CRC). In the present study, we investigated the expression of microRNA-520d-5p (miR-520d-5p) in CRC specimens and then explored its potential role and mechanism in CRC progression. We found that miR-520d-5p was markedly down-regulated in CRC clinical specimens compared with adjacent normal tissues by real-time PCR. Dual-luciferase assays confirmed that miR-520d-5p directly targeting CTHRC1 and SP1 transactivate miR-520d-5p by binding to its upstream promoter region. The biological functional experiments showed that ectopic re-expression of miR-520d-5p suppressed CRC cell proliferation, migration and invasion, whereas the inhibition of miR-520d-5p displayed an inverse effect in vitro and in vivo. Western blot shown that miR-520d-5p abrogated the epithelial-mesenchymal transition by inactivating the phosphorylation of Erk1/2. In conclusion, our findings indicate that miR-520d-5p is significantly down-expressed and involved in CRC progression and metastasis by targeting CTHRC1 and regulated by SP1, which provide new support for miR-520d-5p maybe as a novel anti-onco molecular target for the treatment of CRC in the future.

Indexed as

Colorectal cancerCTHRC1EMTmicroRNA-520d-5pp-Erk1/2SP1

Identifiers

PMID26101709
PMCPMC4473322
OpenAlexW2406942519

What OpenQuestion holds

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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.