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乳腺癌重编程中的代谢途径:非编码 RNA 的新视角。

Metabolic Pathways in Breast Cancer Reprograming: An Insight to Non-Coding RNAs.

机构信息

Immunology Research Center, Tabriz University of Medical Sciences, Tabriz 51666-14731, Iran.

Department of Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz 51666-16471, Iran.

出版信息

Cells. 2022 Sep 23;11(19):2973. doi: 10.3390/cells11192973.


DOI:10.3390/cells11192973
PMID:36230935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9563138/
Abstract

Cancer cells reprogram their metabolisms to achieve high energetic requirements and produce precursors that facilitate uncontrolled cell proliferation. Metabolic reprograming involves not only the dysregulation in glucose-metabolizing regulatory enzymes, but also the enzymes engaging in the lipid and amino acid metabolisms. Nevertheless, the underlying regulatory mechanisms of reprograming are not fully understood. Non-coding RNAs (ncRNAs) as functional RNA molecules cannot translate into proteins, but they do play a regulatory role in gene expression. Moreover, ncRNAs have been demonstrated to be implicated in the metabolic modulations in breast cancer (BC) by regulating the metabolic-related enzymes. Here, we will focus on the regulatory involvement of () in BC metabolism, including glucose, lipid and glutamine metabolism. Investigation of this aspect may not only alter the approaches of BC diagnosis and prognosis, but may also open a new avenue in using ncRNA-based therapeutics for BC treatment by targeting different metabolic pathways.

摘要

癌细胞重新编程其代谢以实现高能量需求,并产生有利于不受控制的细胞增殖的前体。代谢重编程不仅涉及葡萄糖代谢调节酶的失调,还涉及参与脂质和氨基酸代谢的酶。然而,重编程的潜在调节机制尚未完全阐明。非编码 RNA(ncRNA)作为功能性 RNA 分子不能翻译成蛋白质,但它们在基因表达的调控中发挥作用。此外,已经证明 ncRNA 通过调节代谢相关酶参与乳腺癌(BC)的代谢调节。在这里,我们将重点介绍()在 BC 代谢中的调节作用,包括葡萄糖、脂质和谷氨酰胺代谢。研究这一方面不仅可能改变 BC 诊断和预后的方法,而且还可能通过针对不同代谢途径为 BC 治疗开辟使用基于 ncRNA 的治疗的新途径。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ffc/9563138/54ebf3bba2c5/cells-11-02973-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ffc/9563138/df08099d970f/cells-11-02973-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ffc/9563138/54ebf3bba2c5/cells-11-02973-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ffc/9563138/df08099d970f/cells-11-02973-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ffc/9563138/54ebf3bba2c5/cells-11-02973-g002.jpg

相似文献

[1]
Metabolic Pathways in Breast Cancer Reprograming: An Insight to Non-Coding RNAs.

Cells. 2022-9-23

[2]
The emerging regulatory roles of non-coding RNAs associated with glucose metabolism in breast cancer.

Semin Cancer Biol. 2023-10

[3]
Non-coding RNAs derailed: The many influences on the fatty acid reprogramming of cancer.

Life Sci. 2019-5-29

[4]
Roles of non-coding RNAs in the metabolism and pathogenesis of bladder cancer.

Hum Cell. 2023-7

[5]
Metabolism-regulating non-coding RNAs in breast cancer: roles, mechanisms and clinical applications.

J Biomed Sci. 2024-2-26

[6]
Non-coding RNAs in the reprogramming of glucose metabolism in cancer.

Cancer Lett. 2018-1-31

[7]
Non-Coding RNA as Biomarkers and Their Role in the Pathogenesis of Gastric Cancer-A Narrative Review.

Int J Mol Sci. 2024-5-9

[8]
Non-coding RNA in cancer.

Essays Biochem. 2021-10-27

[9]
The role of noncoding RNAs in metabolic reprogramming of cancer cells.

Cell Mol Biol Lett. 2023-5-9

[10]
Vitamin D and Non-coding RNAs: New Insights into the Regulation of Breast Cancer.

Curr Mol Med. 2021

引用本文的文献

[1]
Non-coding RNAs: emerging biomarkers and therapeutic targets in cancer and inflammatory diseases.

Front Oncol. 2025-3-10

[2]
Transmembrane Amino Acid Transporters in Shaping the Metabolic Profile of Breast Cancer Cell Lines: The Focus on Molecular Biological Subtype.

Curr Issues Mol Biol. 2024-12-25

[3]
SIRT4 in ageing.

Biogerontology. 2023-6

本文引用的文献

[1]
MiRNA expression profiling in adenocarcinoma and squamous cell lung carcinoma reveals both common and specific deregulated microRNAs.

Medicine (Baltimore). 2022-8-19

[2]
Long non‑coding RNA CASC11 interacts with YBX1 to promote prostate cancer progression by suppressing the p53 pathway.

Int J Oncol. 2022-9

[3]
Reduced miR-371b-5p expression drives tumor progression via CSDE1/RAC1 regulation in triple-negative breast cancer.

Oncogene. 2022-5

[4]
Knockdown of circ_0102273 inhibits the proliferation, metastasis and glycolysis of breast cancer through miR-1236-3p/PFKFB3 axis.

Anticancer Drugs. 2022-4-1

[5]
STK25 enhances hepatocellular carcinoma progression through the STRN/AMPK/ACC1 pathway.

Cancer Cell Int. 2022-1-5

[6]
Silencing of HMGA2 by siRNA Loaded Methotrexate Functionalized Polyamidoamine Dendrimer for Human Breast Cancer Cell Therapy.

Genes (Basel). 2021-7-20

[7]
MicroRNA-216b targets to potentiate autophagy and apoptosis of breast cancer cells the mTOR signaling pathway.

Int J Biol Sci. 2021-7-13

[8]
Silencing of circHIPK3 Sensitizes Paclitaxel-Resistant Breast Cancer Cells to Chemotherapy by Regulating HK2 Through Targeting miR-1286.

Cancer Manag Res. 2021-7-12

[9]
The expression of miR-513c and miR-3163 was downregulated in tumor tissues compared with normal adjacent tissue of patients with breast cancer.

BMC Med Genomics. 2021-7-7

[10]
CircARL8B Contributes to the Development of Breast Cancer Via Regulating miR-653-5p/HMGA2 Axis.

Biochem Genet. 2021-12

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