Evidence map›Paper›PMID 31700144›Full record

ArticleCell death and differentiation2020

A novel LncRNA HITT forms a regulatory loop with HIF-1α to modulate angiogenesis and tumor growth.

Xingwen Wang, Li Li, Kunming Zhao, Qingyu Lin, Huayi Li, Xuting Xue, Wenjie Ge, Hongjuan He, Dong Liu, Hui Xie and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell death and differentiation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

73 citing papers in PubMed, 115 citations in OpenAlex.

  1. Review
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  4. miR‑205: A dual regulator of angiogenesis in health and disease (Review).International journal of molecular medicine · 2026
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13 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 1 country.

Xingwen WangSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Li LiThe Affiliated Tumor Hospital of Harbin Medical University, 150001, Harbin, Heilongjiang Province, China.
Kunming ZhaoSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Qingyu LinSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Huayi LiSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Xuting XueSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Wenjie GeSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Hongjuan HeSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Dong LiuSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Hui XieState Key Laboratory of Robotics and Systems, Harbin Institute of Technology, 2 Yikuang, 150001, Harbin, China.
Qiong WuSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China.
Ying HuSchool of Life Science and Technology, Harbin Institute of Technology, 150001, Harbin, Heilongjiang Province, China. huying@hit.edu.cn.ORCID http://orcid.org/0000-0003-2469-5604
Harbin Institute of Technology · CNHarbin Medical University · CNShenzhen Institute of Information Technology · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence has indicated that long noncoding RNAs (lncRNAs) play important roles in human diseases, including cancer; however, only a few of them have been experimentally validated and functionally annotated. Here, we identify a novel lncRNA that we term HITT (HIF-1α inhibitor at translation level). HITT is commonly decreased in multiple human cancers. Decreased HITT is associated with advanced stages of colon cancer. Restoration of the expression of HITT in cancer cells inhibits angiogenesis and tumor growth in vivo in an HIF-1α-dependent manner. Further study reveals that HITT inhibits HIF-1α expression, mainly by interfering with its translation. Mechanically, HITT titrates away YB-1 from the 5'-UTR of HIF-1α mRNA via a high-stringency YB-1-binding motif. The reverse correlation between HITT and HIF-1α expression is further validated in human colon cancer tissues. Moreover, HITT is one of the most altered lncRNAs upon the hypoxic switch and HITT downregulation is required for hypoxia-induced HIF-1α expression. We further demonstrate that HITT and HIF-1α form an autoregulatory feedback loop where HIF-1α destabilizes HITT by inducing MiR-205, which directly targets HITT for degradation. Together, these results expand our understanding of the cancer-associated functions of lncRNAs, highlighting the HITT-HIF-1α axis as constituting an additional layer of regulation of angiogenesis and tumor growth, with potential implications for therapeutic targeting.

Indexed as

AnimalsBase SequenceCell Line, TumorCell ProliferationDown-RegulationFeedback, PhysiologicalFemaleGene Expression Regulation, NeoplasticHumansHypoxia-Inducible Factor 1, alpha SubunitMice, NudeMicroRNAsNeoplasmsNeovascularization, PathologicProtein BiosynthesisRNA, Long NoncodingHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitMicroRNAsMIR205, humanRNA, Long NoncodingVascular Endothelial Growth Factor AY-Box-Binding Protein 1YBX1 protein, human

Identifiers

PMID31700144
PMCPMC7205893
OpenAlexW2983156081

What OpenQuestion holds

Textmetadata
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.