Table 2.
The atlas | Methodology | Key findings | References | |
---|---|---|---|---|
Cancer specific | Spatial atlas of LUAD evolution | Single-cell RNA sequencing | Deciphered the geospatial evolution of cellular lineages, states and transcriptional features from normal tissue to LUAD. They also found that CD24 can mediate protumor phenotypes | [201] |
Ecosystem atlas in breast cancer | Single-cell RNA sequencing | Constructed the transcriptional atlas of the evolution trajectory from normal breast and preneoplastic BRCA1( ±) tissue to various subtypes of breast cancer, highlighting the significant heterogeneity in microenvironment | [202, 203] | |
Infiltrated B cells in TNBC | Single-cell RNA sequencing and antigen receptor profiling | The presence of infiltrated B lymphocytes indicated the local differentiation within breast tumors and revealed the positive correlation between B cells and survival via potential immunosurveillance | [204] | |
T cell atlas in gliomas | Single-cell RNA sequencing | Provided the landscape of tumor-infiltrating T cells of IDH wild-type and mutation glioma and identified CD161 as an immunotherapy target | [205] | |
Immune cell atlas in PDAC | Single-cell RNA sequencing | Established the immune cell atlas in PDAC, which acts as a reference to evaluate the immune landscape and potential effect of immunotherapy | [71] | |
Immune cell atlas in ESCC | Single-cell RNA sequencing and TCR sequencing | Demonstrated the dynamics of various immune cells along tumor progression and indicated several immunosuppressive mechanisms | [206] | |
Cellular hierarchy atlas in AML | Microwell-Seq and SMRT-seq | Revealed the AML landscape and proposed a ‘cancer attractor’ phenotype, which may help define the AML progenitor cell associated with prognosis | [69] | |
Pancancer atlas | CancerSEA | Single-cell RNA sequencing | Provided a user-friendly database of 14 functional states of tumor cells (including stemness, invasion and EMT). It also provided the functional states associated PCG/lncRNA repertoires among cancers | [207] |
CD8 + T cell atlas | Transposase-accessible chromatin sequencing, RNA sequencing | Defined the differentiation trajectory of CD8 + T cells toward dysfunction and revealed the underlying transcriptional drivers across various tumors, including melanoma and HCC | [208] | |
TIM atlas | Single-cell RNA sequencing | Revealed the similarity and distinction of TIMs, including mast cells, DCs and TAMs, across 15 tumors and revealed the association with somatic mutations and gene expression | [209] | |
HLA atlas | Immunoaffinity purification and liquid chromatography mass spectrometry | Delineated the HLA-I and HLA-II immunopeptidomes from tumor and benign human tissue samples, enabling the balanced comparison of HLA ligand levels and thus facilitating immunotherapy | [210] | |
Fibroblast atlas | Single-cell RNA sequencing | Demonstrated that fibroblast transcriptional states are conservative across species and in different diseases | [211] |
LUAD: lung adenocarcinoma; IDH: isocitrate dehydrogenase; TIM: tumor-infiltrating myeloid cells; TAM: tumor-infiltrating macrophages; HLA: human leucocyte antigen; PDAC: pancreatic ductal adenocarcinoma; TNBC: triple-negative breast cancer; ESCC: esophageal squamous cell carcinoma; AML: acute myeloid leukemia; SMRT-seq: single-cell single-molecule real-time sequencing