Evidence map›Paper›PMID 32239427›Full record

ArticleClinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico2020

RUNX1-activated upregulation of lncRNA RNCR3 promotes cell proliferation, invasion, and suppresses apoptosis in colorectal cancer via miR-1301-3p/AKT1 axis in vitro and in vivo.

G Xu, H Wang, D Yuan, J Yao, L Meng, K Li, Y Zhang, C Dang, K Zhu

Abstract read
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In one paragraph

Article in Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.8field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 57 citations in OpenAlex.

  1. Article
  2. Serums miR-24-3p and miR-1301-3p as Potential Biomarkers in MEN1 Syndrome.International journal of molecular sciences · 2025
    Article
  3. Review
  4. Article
  5. Exploring the Key Signaling Pathways and ncRNAs in Colorectal Cancer.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Potentials of long non-coding RNAs as biomarkers of colorectal cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  12. 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

9 authors at 1 institution in 1 country.

G XuDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China. gxxajt2019@yeah.net.ORCID http://orcid.org/0000-0002-6236-7823
H WangDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
D YuanDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
J YaoDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
L MengDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
K LiDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
Y ZhangDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
C DangDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
K ZhuDepartment of Surgical Oncology, The First Affiliated Hospital of Xi'an Jiao Tong University, 277 West Yan-ta Road, Xi 'an, 710061, Shaanxi, People's Republic of China.
First Affiliated Hospital of Xi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLong non-coding RNAs (lncRNAs) have participated in progression of colorectal cancer. This study aims to study the role of RUNX1/RNCR3/miR-1301-3p/AKT1 axis in colorectal cancer.

methodsThe cancer tissues were from patients with colorectal cancer. The qRT-PCR was used to determine expression of lncRNA RNCR3, miR-1301-3p, and AKT1. Both dual-luciferase reporter assay and ChIP assay were conducted to investigate the binding sites of RUNX1 on RNCR3 promoter. Western blot was performed to analyze expression of AKT1 protein. Both dual-luciferase reporter assay and RIP assay were performed to detect the interacting sites between RNCR3 and miR-1301-3p. The CCK-8 assay, soft agar assay, transwell assay, and annexin-V-FITC/PI staining were applied to analyze the cell growth, invasion, and apoptosis, respectively.

resultsThe data demonstrated that RNCR3 was elevated in colorectal cancer, and it was negatively correlated with expression of miR-1301-3p which was decreased in cancers. Then, RNCR3 could interact with and suppress miR-1301-3p expression in HCT116 and SW480. Knockdown of RNCR3 or miR-1301-3p overexpression significantly inhibited cell growth, invasion, and increased apoptosis through suppressing expression of Cyclin A1, PCNA, N-cadherin, Bcl-2, and promoting expression of E-cadherin, Bax in vitro and in vivo. RUNX1 was directly bound to RNCR3 promoter to activate RNCR3 expression. Furthermore, overexpression of RNCR3 blocked tumor inhibitory effects of miR-1301-3p on proliferation, colony formation, invasion, and apoptosis in vitro and in vivo. Additionally, RNCR3 and miR-1301-3p synergistically modulated AKT1 expression.

conclusionRUNX1-activated upregulation of RNCR3 promoted colorectal cancer progression by sponging miR-1301-3p to elevate AKT1 levels in vitro and in vivo.

Indexed as

ApoptosisAnimalsCell Line, TumorCell MovementCell ProliferationColorectal NeoplasmsCore Binding Factor Alpha 2 SubunitDisease ProgressionFemaleHumansMiceMice, Inbred BALB CMicroRNAsNeoplasm InvasivenessPromoter Regions, GeneticProto-Oncogene Proteins c-aktCore Binding Factor Alpha 2 Subunitlong non-coding RNA RNCR3, humanMicroRNAsMIRN1301 microRNA, humanProto-Oncogene Proteins c-aktRNA, Long NoncodingRUNX1 protein, humanAKT1Colorectal cancermiR-1301-3pRNCR3RUNX1

Identifiers

PMID32239427
OpenAlexW3014531695

What OpenQuestion holds

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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.