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HOXC Cluster Antisense RNA 3, a Novel Long Non-Coding RNA as an Oncological Biomarker and Therapeutic Target in Human Malignancies.

作者信息

Xie Yunhe, Ye Jiarong, Luo Hongliang

机构信息

Department of Gastrointestinal Surgery, The Second Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, 330008, People's Republic of China.

Department of General Surgery, Jiujiang Hospital of Traditional Chinese Medicine, Jiujiang, Jiangxi, 332007, People's Republic of China.

出版信息

Onco Targets Ther. 2023 Oct 24;16:849-865. doi: 10.2147/OTT.S425523. eCollection 2023.


DOI:10.2147/OTT.S425523
PMID:37899986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10612484/
Abstract

HOXC cluster antisense RNA 3 (HOXC-AS3) is a novel long noncoding RNA (lncRNA) that exhibits aberrant expression patterns in various cancer types. Its expression is closely related to clinicopathological features, demonstrating significant clinical relevance across multiple tumors. And HOXC-AS3 plays multifaceted roles in tumor progression, impacting cell proliferation, apoptosis, migration, invasion, epithelial-mesenchymal transition (EMT), autophagy, senescence, tumor growth, and metastasis. In this review, we summarized and comprehensively analyzed the expression and clinical significance of HOXC-AS3 as a diagnostic and prognostic biomarker for malignancies. Additionally, we presented an in-depth update on HOXC-AS3's functions and regulatory mechanisms in cancer pathogenesis. This narrative review underscores the importance of HOXC-AS3 as a promising lncRNA candidate in cancer research and its potential as a predictive biomarker and therapeutic target in clinical applications.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/4ffd89a201e0/OTT-16-849-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/10cf9a740f47/OTT-16-849-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/fbf78717467d/OTT-16-849-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/d8cbc12a25b9/OTT-16-849-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/37eb87f43e30/OTT-16-849-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/38ca7dc2a099/OTT-16-849-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/3532c3c9316f/OTT-16-849-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/969d8a79fd47/OTT-16-849-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/4ffd89a201e0/OTT-16-849-g0008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/10cf9a740f47/OTT-16-849-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/fbf78717467d/OTT-16-849-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/d8cbc12a25b9/OTT-16-849-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/37eb87f43e30/OTT-16-849-g0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/38ca7dc2a099/OTT-16-849-g0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/3532c3c9316f/OTT-16-849-g0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/969d8a79fd47/OTT-16-849-g0007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/836f/10612484/4ffd89a201e0/OTT-16-849-g0008.jpg

相似文献

[1]
HOXC Cluster Antisense RNA 3, a Novel Long Non-Coding RNA as an Oncological Biomarker and Therapeutic Target in Human Malignancies.

Onco Targets Ther. 2023-10-24

[2]
LncRNA HOXC-AS3 overexpression inhibits TGF-β2-induced colorectal cancer cell migration and invasion by sponging miR-1269.

Hum Exp Toxicol. 2022

[3]
LncRNA HOXC-AS3 accelerates malignant proliferation of cervical cancer cells via stabilizing KDM5B.

J Cancer Res Clin Oncol. 2024-6-6

[4]
The Long Non-Coding RNA HOXC-AS3 Promotes Glioma Progression by Sponging miR-216 to Regulate F11R Expression.

Front Oncol. 2022-3-23

[5]
LncRNA HOXC-AS3 increases non-small cell lung cancer cell migration and invasion by sponging premature miR-96.

Expert Rev Respir Med. 2022-5

[6]
Long noncoding RNA HOXC-AS3 facilitates the progression of invasive mucinous adenocarcinomas of the lung via modulating FUS/FOXM1.

In Vitro Cell Dev Biol Anim. 2020-1-10

[7]
Long noncoding RNA HOXC-AS3 indicates a poor prognosis and regulates tumorigenesis by binding to YBX1 in breast cancer.

Am J Transl Res. 2020-10-15

[8]
LncRNA HOXC-AS3 promotes non-small-cell lung cancer growth and metastasis through upregulation of YBX1.

Cell Death Dis. 2022-4-6

[9]
A Novel lncRNA HOXC-AS3 Acts as a miR-3922-5p Sponge to Promote Breast Cancer Metastasis.

Cancer Invest. 2019-12-4

[10]
A concise review of the regulatory, diagnostic, and prognostic implications of HOXB-AS3 in tumors.

J Cancer. 2024-1-1

引用本文的文献

[1]
Long Noncoding RNA VLDLR-AS1 Levels in Serum Correlate with Combat-Related Chronic Mild Traumatic Brain Injury and Depression Symptoms in US Veterans.

Int J Mol Sci. 2024-1-25

本文引用的文献

[1]
lncRNA cytoskeleton regulator RNA (CYTOR): Diverse functions in metabolism, inflammation and tumorigenesis, and potential applications in precision oncology.

Genes Dis. 2021-10-23

[2]
Roles of non-coding RNAs in the metabolism and pathogenesis of bladder cancer.

Hum Cell. 2023-7

[3]
Multiple therapeutic approaches of glioblastoma multiforme: From terminal to therapy.

Biochim Biophys Acta Rev Cancer. 2023-7

[4]
Amino acid metabolism regulated by lncRNAs: the propellant behind cancer metabolic reprogramming.

Cell Commun Signal. 2023-5-1

[5]
Non‑coding RNAs: Role of miRNAs and lncRNAs in the regulation of autophagy in hepatocellular carcinoma (Review).

Oncol Rep. 2023-6

[6]
Epigenetic programing of cancer stemness by transcription factors-non-coding RNAs interactions.

Semin Cancer Biol. 2023-7

[7]
The role of long non-coding RNAs in carbohydrate and fat metabolism in the liver.

Noncoding RNA Res. 2023-3-14

[8]
Postoperative survival of pulmonary invasive mucinous adenocarcinoma versus non-mucinous invasive adenocarcinoma.

BMC Pulm Med. 2023-1-9

[9]
Long non-coding RNAs: definitions, functions, challenges and recommendations.

Nat Rev Mol Cell Biol. 2023-6

[10]
LncRNA HOXA11-AS promotes glioma malignant phenotypes and reduces its sensitivity to ROS via Tpl2-MEK1/2-ERK1/2 pathway.

Cell Death Dis. 2022-11-9

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