Evidence map›Paper›PMID 39227375›Full record

ArticleCell death & disease2024

HIF1A-AS2 promotes the metabolic reprogramming and progression of colorectal cancer via miR-141-3p/FOXC1 axis.

Xinyang Zhong, Yaxian Wang, Xuefeng He, Xinxin He, Zijuan Hu, Huixia Huang, Jiayu Chen, Keji Chen, Ping Wei, Senlin Zhao and 4 more

Abstract read
In one paragraph

Article in Cell death & disease, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
–field-weighted citation impact
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

19 citing papers in PubMed.

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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

14 authors.

Xinyang Zhong *Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yaxian Wang *Department of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Xuefeng He *Cancer Institute, ZJU-UCLA Joint Center for Medical Education and Research, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Xinxin He *Department of Gastrointestinal Surgery, Guangxi Medical University Cancer Hospital, Nanning, China.
Zijuan HuDepartment of Oncology, Shanghai Medical College Fudan University, Shanghai, China.
Huixia HuangDepartment of Oncology, Shanghai Medical College Fudan University, Shanghai, China.
Jiayu ChenDepartment of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Keji ChenDepartment of Oncology, Shanghai Medical College Fudan University, Shanghai, China.
Ping WeiDepartment of Oncology, Shanghai Medical College Fudan University, Shanghai, China.ORCID 0000-0002-9805-6330
Senlin ZhaoDepartment of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China.
Yilin WangDepartment of Oncology, Shanghai Medical College Fudan University, Shanghai, China. linglingwangyi@126.com.
Hong ZhangColorectal Tumor Surgery Ward, Department of General Surgery, Shengjing Hospital of China Medical University, Shenyang, China. haojiubujian1203@sina.cn.
Bo FengDepartment of General Surgery, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China. fb11427@rjh.com.cn.
Dawei LiDepartment of Colorectal Surgery, Fudan University Shanghai Cancer Center, Shanghai, China. li_dawei@fudan.edu.cn.ORCID 0000-0002-5642-4000

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81972185National Natural Science Foundation of China (National Science Foundation of China) 81972293
6 · The paper itself

Abstract

lncRNA can regulate tumorigenesis development and distant metastasis of colorectal cancer (CRC). However, the detailed molecular mechanisms are still largely unknown. Using RNA-sequencing data, RT-qPCR, and FISH assay, we found that HIF1A-AS2 was upregulated in CRC tissues and associated with poor prognosis. Functional experiments were performed to determine the roles of HIF1A-AS2 in tumor progression and we found that HIF1A-AS2 can promote the proliferation, metastasis, and aerobic glycolysis of CRC cells. Mechanistically, HIF1A-AS2 can promote FOXC1 expression by sponging miR-141-3p. SP1 can transcriptionally activate HIF1A-AS2. Further, HIF1A-AS2 can be packaged into exosomes and promote the malignant phenotype of recipient tumor cells. Taken together, we discovered that SP1-induced HIF1A-AS2 can promote the metabolic reprogramming and progression of CRC via miR-141-3p/FOXC1 axis. HIF1A-AS2 is a promising diagnostic marker and treatment target in CRC.

Indexed as

Colorectal NeoplasmsDisease ProgressionForkhead Transcription FactorsGene Expression Regulation, NeoplasticMicroRNAsAnimalsCell Line, TumorCell MovementCell ProliferationFemaleGlycolysisHumansHypoxia-Inducible Factor 1, alpha SubunitMaleMetabolic ReprogrammingMiceForkhead Transcription FactorsHypoxia-Inducible Factor 1, alpha Subunitlong noncoding RNA HIF1A-AS2, humanMicroRNAsMIRN141 microRNA, humanRNA, Long NoncodingSP1 protein, humanSp1 Transcription Factor

Identifiers

PMID39227375
PMCPMC11372083

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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.