Evidence map›Paper›PMID 30881029›Full record

ArticleOncoTargets and therapy2019

Upregulated expression of ACTL8 contributes to invasion and metastasis and indicates poor prognosis in colorectal cancer.

Qiang Han, Ming-Li Sun, Wen-Si Liu, Hai-Shan Zhao, Long-Yang Jiang, Zhao-Jin Yu, Min-Jie Wei

Open access · goldAbstract read
In one paragraph

Article in OncoTargets and therapy, 2019. 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
1.2field-weighted citation impact, top 22% 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, 18 citations in OpenAlex.

  1. Establishment of insulin resistance-related ten-gene signature in endometrial cancer and identification of ACTL8 as a prognostic and immunological biomarker.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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.

Qiang HanDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang 110122, Liaoning, China, weiminjiecmu@163.com; yuzhaojin19830813@163.com.
Ming-Li SunDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang 110122, Liaoning, China, weiminjiecmu@163.com; yuzhaojin19830813@163.com.
Wen-Si LiuDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang 110122, Liaoning, China, weiminjiecmu@163.com; yuzhaojin19830813@163.com.
Hai-Shan ZhaoDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang 110122, Liaoning, China, weiminjiecmu@163.com; yuzhaojin19830813@163.com.
Long-Yang JiangDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang 110122, Liaoning, China, weiminjiecmu@163.com; yuzhaojin19830813@163.com.
Zhao-Jin YuDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang 110122, Liaoning, China, weiminjiecmu@163.com; yuzhaojin19830813@163.com.
Min-Jie WeiDepartment of Pharmacology, School of Pharmacy, China Medical University, Shenyang 110122, Liaoning, China, weiminjiecmu@163.com; yuzhaojin19830813@163.com.
China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundACTL8 is a member of the CT antigens. There are only few studies on the role of ACTL8 in malignant tumors. The aim of this study is to investigate the expression and clinical significance of ACTL8 protein in colorectal cancer (CRC). MATERIALS AND

methodsHuman CRC tissues and cell lines, and paired adjacent non-tumor tissues and human intestinal epithelial cell lines were obtained to evaluate the expression of ACTL8. The association between protein expression of ACTL8 and clinicopathological parameters and prognosis of CRC patients was examined. The biological functions of ACTL8 in the invasion and metastasis of CRC were determined by wound healing and transwell invasion assays after silencing of ACTL8 in CRC cell lines. The potential target genes of ACTL8 were also identified by quantitative reverse transcription PCR and Western blotting after silencing of ACTL8 in CRC cell lines.

resultsIt was found that ACTL8 was upregulated in human CRC tissues and cell lines. The expression of ACTL8 was positively associated with poor differentiation, invasion and metastasis, postoperative infection, and poor prognosis, but negatively associated with proximal margin length. In addition, silencing of ACTL8 significantly decreased the capacity of invasion and migration in HT29 and SW620 CRC cell lines. Moreover, silencing of ACTL8 significantly decreased the expression of TRIM29 in HT29 and SW620 CRC cell lines.

conclusionThese results suggest that ACTL8 plays a key role in the invasion and metastasis of CRC, and TRIM29 may be involved in the ACTL8-mediated poor prognosis of CRC.

Indexed as

ACTL8CRCinvasion and metastasisprognosisTRIM29

Identifiers

PMID30881029
PMCPMC6402434
OpenAlexW2916955991

What OpenQuestion holds

Textmetadata
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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.