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Article: Applications and Prospects of Single-Cell RNA Sequencing and Spatial Transcriptomics in Cervical Cancer

TitleApplications and Prospects of Single-Cell RNA Sequencing and Spatial Transcriptomics in Cervical Cancer
Authors
Keywordscervical cancer
single-cell RNA sequencing
spatial transcriptomics
therapeutic targets
tumor microenvironment
Issue Date1-Jan-2025
PublisherHindawi
Citation
BioMed Research International, 2025, v. 2025, n. 1 How to Cite?
AbstractCervical cancer (CC) is the fourth commonest malignant tumor among women worldwide and is characterized by high heterogeneity and a complex ecosystem. A comprehensive understanding of the heterogeneity of tumors and the tumor microenvironment (TME) is crucial for effective CC management. Single-cell RNA sequencing (scRNA-seq) is a powerful tool that can be employed to unveil the heterogeneity of tumors and the TME, as well as to elucidate the evolutionary trajectories of tumors. Spatial transcriptomics (ST) technology, on the other hand, can address the complexity and diversity of the spatial microenvironment of tumors, thereby compensating for the limitations of scRNA-seq. As emerging technologies, both scRNA-seq and ST are increasingly being utilized in CC research. In this review, we summarized the latest advancements in scRNA-seq and ST for CC, with a focus on investigating tumor heterogeneity, the TME, tumor evolutionary trajectories, treatment resistance mechanisms, and potential therapeutic targets. These insights collectively contribute to the development of more effective treatment and prevention strategies for CC.
Persistent Identifierhttp://hdl.handle.net/10722/357845
ISSN
2023 Impact Factor: 2.6
2023 SCImago Journal Rankings: 0.656
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorWang, Yifu-
dc.contributor.authorYang, Li-
dc.contributor.authorLiu, Yunzhi-
dc.contributor.authorMa, Huangrong-
dc.contributor.authorCai, Miaoying-
dc.contributor.authorLiang, Chunyu-
dc.contributor.authorZhang, Li-
dc.contributor.authorSu, Zezhuo-
dc.contributor.authorXu, Zhiyuan-
dc.date.accessioned2025-07-22T03:15:18Z-
dc.date.available2025-07-22T03:15:18Z-
dc.date.issued2025-01-01-
dc.identifier.citationBioMed Research International, 2025, v. 2025, n. 1-
dc.identifier.issn2314-6133-
dc.identifier.urihttp://hdl.handle.net/10722/357845-
dc.description.abstractCervical cancer (CC) is the fourth commonest malignant tumor among women worldwide and is characterized by high heterogeneity and a complex ecosystem. A comprehensive understanding of the heterogeneity of tumors and the tumor microenvironment (TME) is crucial for effective CC management. Single-cell RNA sequencing (scRNA-seq) is a powerful tool that can be employed to unveil the heterogeneity of tumors and the TME, as well as to elucidate the evolutionary trajectories of tumors. Spatial transcriptomics (ST) technology, on the other hand, can address the complexity and diversity of the spatial microenvironment of tumors, thereby compensating for the limitations of scRNA-seq. As emerging technologies, both scRNA-seq and ST are increasingly being utilized in CC research. In this review, we summarized the latest advancements in scRNA-seq and ST for CC, with a focus on investigating tumor heterogeneity, the TME, tumor evolutionary trajectories, treatment resistance mechanisms, and potential therapeutic targets. These insights collectively contribute to the development of more effective treatment and prevention strategies for CC.-
dc.languageeng-
dc.publisherHindawi-
dc.relation.ispartofBioMed Research International-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.subjectcervical cancer-
dc.subjectsingle-cell RNA sequencing-
dc.subjectspatial transcriptomics-
dc.subjecttherapeutic targets-
dc.subjecttumor microenvironment-
dc.titleApplications and Prospects of Single-Cell RNA Sequencing and Spatial Transcriptomics in Cervical Cancer-
dc.typeArticle-
dc.identifier.doi10.1155/bmri/1532745-
dc.identifier.scopuseid_2-s2.0-105009206317-
dc.identifier.volume2025-
dc.identifier.issue1-
dc.identifier.eissn2314-6141-
dc.identifier.isiWOS:001517508100001-
dc.identifier.issnl2314-6133-

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