Evidence map›Paper›PMID 32801872›Full record

ArticleCancer management and research2020

FOXCUT Promotes the Proliferation and Invasion by Activating FOXC1/PI3K/AKT Pathway in Colorectal Cancer.

Xiaojie Zhang, Shanyong Yi, Guochen Xing, Huili Wu, Ying Zhu, Xiaodan Guo, Lei Zhang

Open access · goldAbstract read
In one paragraph

Article in Cancer management and research, 2020. 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
0.5field-weighted citation impact, top 44% 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, 10 citations in OpenAlex.

  1. Article
  2. The Role of the Fox Gene in Breast Cancer Progression.International journal of molecular sciences · 2025
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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

7 authors at 1 institution in 1 country.

Xiaojie ZhangZhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, People's Republic of China.
Shanyong YiZhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, People's Republic of China.
Guochen XingZhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, People's Republic of China.
Huili WuZhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, People's Republic of China.
Ying ZhuZhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, People's Republic of China.
Xiaodan GuoZhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, People's Republic of China.
Lei ZhangZhengzhou Central Hospital Affiliated to Zhengzhou University, Zhengzhou 450000, People's Republic of China.
Zhengzhou Central Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionColorectal cancer (CRC) is the third most commonly diagnosed world cancer. Long noncoding RNAs (lncRNAs) serve important regulatory roles in tumorigenesis. However, the contributions of lncRNAs to human CRC remain largely unknown. MATERIAL AND

methodsFOXC1 and FOXCUT lncRNA expression levels were detected in a panel of paired specimens obtained from 48 patients' tissues and cell lines with CRC using RT-qPCR. RNA interference was used to investigate potential correlations between FOXC1 and FOXCUT expression in HT29. Cell proliferation was assessed by MTT assay and EdU incorporation assay. The migration and invasion of CRC cells were detected by transwell assay. Western blot was applied to assess the protein expression and PI3K/AKT signaling pathway.

resultsIn this study, a novel long noncoding RNA (FOXCUT) was frequently overexpressed in CRC tissues and cell lines. In addition, the expressions of FOXCUT and FOXC1 were positively correlated. When the expression of FOXCUT was downregulated by small interfering RNA (siRNA), the expression of FOXC1 was also decreased. Moreover, knockdown of FOXCUT significantly inhibited proliferation and invasion of CRC cell lines and resulted in downregulated expression of the matrix metalloproteinase 1 (MMP-1). Mechanistically, FOXCUT promotes the expression of FOXC1 to activate PI3K/AKT signaling pathway for its regulation of cell growth and proliferation.

conclusionIn summary, our findings indicate that FOXCUT plays an important oncogenic role and may serve as a novel biomarker and therapeutic target in CRC progression.

Indexed as

colorectal cancerFOXC1FOXCUTinvasionproliferation

Identifiers

PMID32801872
PMCPMC7399466
OpenAlexW3044856686

What OpenQuestion holds

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LicenceCC BY-NC
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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.