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Adenosinergic Signalling in Cervical Cancer Microenvironment.

作者信息

Iser Isabele Cristiana, Bertoni Ana Paula Santin, Beckenkamp Liziane Raquel, Consolaro Marcia Edilaine Lopes, Maria-Engler Silvya Stuchi, Wink Marcia Rosângela

机构信息

Department of Basics Health Sciences and Laboratory of Cell Biology, Federal University of Health Sciences of Porto Alegre, Porto Alegre, RS, Brazil.

Department of Clinical Analysis and Biomedicine, Division of Clinical Cytology, State University of Maringá, Maringá, PR, Brazil.

出版信息

Expert Rev Mol Med. 2025 Jan 7;27:e5. doi: 10.1017/erm.2024.30.


DOI:10.1017/erm.2024.30
PMID:39762204
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11707834/
Abstract

Despite the emergence of the first human papillomavirus vaccine, the incidence of cervical cancer is still responsible for more than 350,000 deaths yearly. Over the past decade, ecto-5'-nucleotidase (CD73/5'-NT) and extracellular adenosine (ADO) signalling has been the subject of many investigations to target cancer progression. In general, the adenosinergic axis has been linked to tumourigenic effects. However, CD73 can play contradictory effects, probably dependent on the tumour type, tumour microenvironment and tumour stage, thus being in some circumstances, inversely related to tumour progression. We herein reviewed the pathophysiological function of CD73 in cervical cancer and performed analysis of the main components of the adenosinergic signalling in human tissues of cervical cancer compared to non-tumour cervix tissue. Our data showed that the gene, that encoded CD73, is hypermethylated, leading to a decreased CD73 expression in cervical cancer cells compared to normal cells. Consequently, the high availability of ADO cytoplasmatic/extracellular leads to its conversion to AMP by ADK, culminating in global hypermethylation. Therefore, epigenetic modulation may reveal a new role for CD73 in cervical cancer.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/f957d7b737f5/S1462399424000309_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/0da063833240/S1462399424000309_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/1dc97a821d75/S1462399424000309_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/1699352fe4e0/S1462399424000309_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/655c4a3f5037/S1462399424000309_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/f69c60fa6490/S1462399424000309_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/896f1ceb4ad3/S1462399424000309_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/e52b4b0cba72/S1462399424000309_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/b2c5dfc9144a/S1462399424000309_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/f957d7b737f5/S1462399424000309_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/0da063833240/S1462399424000309_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/1dc97a821d75/S1462399424000309_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/1699352fe4e0/S1462399424000309_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/655c4a3f5037/S1462399424000309_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/f69c60fa6490/S1462399424000309_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/896f1ceb4ad3/S1462399424000309_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/e52b4b0cba72/S1462399424000309_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/b2c5dfc9144a/S1462399424000309_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1a4d/11707834/f957d7b737f5/S1462399424000309_fig9.jpg

相似文献

[1]
Adenosinergic Signalling in Cervical Cancer Microenvironment.

Expert Rev Mol Med. 2025-1-7

[2]
A three-dimensional microenvironment alters CD73 expression in cervical cancer.

Cell Biochem Funct. 2021-8

[3]
Cervical cancer cells produce TGF-β1 through the CD73-adenosine pathway and maintain CD73 expression through the autocrine activity of TGF-β1.

Cytokine. 2018-10-6

[4]
CD73 promotes proliferation and migration of human cervical cancer cells independent of its enzyme activity.

BMC Cancer. 2017-2-15

[5]
Cervical cancer cells suppress effector functions of cytotoxic T cells through the adenosinergic pathway.

Cell Immunol. 2017-10

[6]
Extracellular adenosine oppositely regulates the purinome machinery in glioblastoma and mesenchymal stem cells.

IUBMB Life. 2024-12

[7]
Alternative splicing of human NT5E in cirrhosis and hepatocellular carcinoma produces a negative regulator of ecto-5'-nucleotidase (CD73).

Mol Biol Cell. 2014-12-15

[8]
Identification and Expression Analysis of CD73 Inhibitors in Cervical Cancer.

Med Chem. 2021

[9]
CD73 acts as a prognostic biomarker and promotes progression and immune escape in pancreatic cancer.

J Cell Mol Med. 2020-8

[10]
The immunomodulatory ballet of tumour-derived extracellular vesicles and neutrophils orchestrating the dynamic CD73/PD-L1 pathway in cancer.

J Extracell Vesicles. 2024-7

引用本文的文献

[1]
TGF-β Induces the Secretion of Extracellular Vesicles Enriched with CD39 and CD73 from Cervical Cancer Cells.

Int J Mol Sci. 2025-3-7

本文引用的文献

[1]
Assessing the distribution of cancer stem cells in tumorspheres.

Sci Rep. 2024-5-14

[2]
Wnt/β-catenin-driven EMT regulation in human cancers.

Cell Mol Life Sci. 2024-2-9

[3]
First-in-human study of SBRT and adenosine pathway blockade to potentiate the benefit of immunochemotherapy in early-stage luminal B breast cancer: results of the safety run-in phase of the Neo-CheckRay trial.

J Immunother Cancer. 2023-12-6

[4]
Paclitaxel plus carboplatin and durvalumab with or without oleclumab for women with previously untreated locally advanced or metastatic triple-negative breast cancer: the randomized SYNERGY phase I/II trial.

Nat Commun. 2023-11-2

[5]
The Clinical Significance of CD73 in Cancer.

Int J Mol Sci. 2023-7-21

[6]
Transcriptional control of pancreatic cancer immunosuppression by metabolic enzyme CD73 in a tumor-autonomous and -autocrine manner.

Nat Commun. 2023-6-8

[7]
NT5E DNA methylation in papillary thyroid cancer: Novel opportunities for precision oncology.

Mol Cell Endocrinol. 2023-6-15

[8]
First-in-human study of oleclumab, a potent, selective anti-CD73 monoclonal antibody, alone or in combination with durvalumab in patients with advanced solid tumors.

Cancer Immunol Immunother. 2023-7

[9]
CD73 in glioblastoma: Where are we now and what are the future directions?

Immunol Lett. 2023

[10]
Inhibition of CD73 expression or A2AR blockade reduces MRP1 expression and increases the sensitivity of cervical cancer cells to cisplatin.

Cell Biochem Funct. 2023-4

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