Researchers | CRGs | The Highlights | References |
---|---|---|---|
Zhen Zhang and his colleagues | FDX1 and related genes(ALDH5A1, CAT, EHHADH, and SLC27A) | CRRS: The high CRRS group showed lower survival and increased tumor immune infiltration | [10] |
Lei Ding and his colleagues | CDKN2A, DLAT, DLD, FDX1, GLS, LIAS, LIPT1, MTF1, PDHA1, and PDHB | 1. Three subtypes of cuproptosis were validated; 2. CRGPI: could be used as a potential biomarker for prognosis and immunotherapy in HCC patients | [112] |
Zhiqiang Liu and his colleagues | ATP7A, ATP7B, DBT, DLAT, DLD, DLST, FDX1, GCSH, LIAS, LIPT1, PDHA1, PDHB, and SLC31A1 | 1. Three subgroups of patients based on CRGs were revealed; 2. A cuproptosis-related prognostic risk model was built to predict prognosis | [113] |
Jie Fu and his colleagues | ATP7A, ATP7B, CDKN2A, DLAT, DLD, FDX1, GCSH, GLS, LIAS, LIPT1, LIPT2, MPC1, MTF1, PDHA1, PDHB, SLC31A1 | 1. Three distinct CRGs expression patterns were identified; 2. CRRS was established to predict the prognosis, the immune microenvironment, and expression of immune checkpoint molecules | [111] |
Tianhao Cong and his colleagues | Cuproptosis-related ICGs (BTN2A1, BTNL9, CD276, CD40LG, LGALS9, SIRPA, TNFRSF4) | Cuproptosis-related ICGs were developed to predict the prognosis and immune response of HCC patients | [114] |
Xi Chen and his colleagues | ATP7A, ATP7B, BAD, PDHA1, CCS, CDKN2A, DLAT, DLD, FDX1, GLS, LIAS, LIPT1, MTF1, MTOR, NRF2, PDHB, and SLC31A1 | 1. Three cuproptosis subtypes were identified; 2. Cuproptosis signature has been built containing five cuproptosis-associated genes: CLEC3B, CFH, HPR, LAMB1, and PFKFB3 | [101] |