Single-cell RNA-sequencing reveals the landscape of cervical cancer heterogeneity
Cervical cancer (CC) is the forth leading cause of deaths in gynecological tumor. Although the etiology of CC has been extensively investigated, the exact pathogenesis of CC remains incomplete. Therefore, we applied single-cell RNA sequencing on cancer tissue and normal adjacent tissue from a patient with CC. Together, we identified four tumor cell subpopulations in tumor cells, which had specific signature genes with different biological functions and presented different prognosis. Among them, we identified a subset of cancer stem cell (CSCs), which was related to the developmental hierarchy of tumor progression. These data facilitate the understanding of the CC landscape and provides deeper insights into the development of prognostic biomarkers and therapeutic targets in the CC.
To reference this project, please use the following link:
Downloaded and exported data is governed by the HCA Data Release Policy and licensed under the Creative Commons Attribution 4.0 International License (CC BY 4.0). For more information please see our Data Use Agreement.
Atlas
Analysis Portals
NoneProject Label
CervicalCancerLandscapeSpecies
Homo sapiens
Sample Type
specimens
Anatomical Entity
uterus
Organ Part
uterine cervix
Selected Cell Types
Unspecified
Disease Status (Specimen)
Disease Status (Donor)
cervical cancer
Development Stage
human adult stage
Library Construction Method
10x 3' V2 sequencing
Nucleic Acid Source
single cell
Paired End
falseAnalysis Protocol
analysis_protocol_1File Format
Cell Count Estimate
UnspecifiedDonor Count
1