Breast cancer |
Expression of APOBEC3B is increased in breast tumors and cell lines. Breast TCGA tumors have a more prevalent APOBEC3B mutation than is expected |
Human tissue samples. In vitro, human cell lines |
[8, 48, 64] |
HER2-enriched subtype of breast cancer has a significantly higher frequency of mutations associated with APOBEC3B than other breast cancer subtypes |
TCGA |
[60] |
APOBEC3B leads to drug resistance in breast cancer and APOBEC3B-dependent tumor evolvability may serve as a effective target to improve efficacies of anti-cancer therapies |
Human tissue samples |
[62, 65] |
APOBEC3B depletion in an ER+ breast cancer cell line results in prolonged tamoxifen response |
Xenograft model |
[66] |
Gastric cancer |
APOBEC3B expression was higher in gastric cancer tissues than that in normal tissues and APOBEC3B overexpression indicates the unfavorable prognosis of the patients with gastric cancer |
Human tissue samples |
[8, 62, 67] |
Chondrosarcoma |
APOBEC3B was overexpressed in chondrosarcoma tissues, and APOBEC3B deficiency caused slight apoptosis in the chondrosarcoma cells |
Human tissue samples. In vitro, human cell lines |
[8, 68] |
Hepatocellular carcinoma |
APOBEC3B was the only APOBEC3 family member significantly overexpressed in hepatocellular carcinoma (HCC) tissues and may be a potential factor contributing to suppression of tumor growth in HCC |
Human tissue samples. In vitro, human cell lines |
[69] |
APOBEC3B is a potential factor contributing to suppression of tumor growth in HCC |
In vitro, human cell lines |
[70] |
Renal cancer |
Renal clear-cell carcinomas showed statistically notable up-regulation of APOBEC3B |
Human tissue samples |
[8, 71] |
Colorectal cancer |
APOBEC3B was overexpressed in colorectal cancer tissues |
Human tissue samples |
[8, 72] |
Prostate cancer |
Prostate carcinomas showed statistically marked up-regulation of APOBEC3B |
Human tissue samples |
[8, 72] |
Cervix cancer |
APOBEC3B was overexpressed in cervix cancer tissues |
Human tissue samples |
[8] |
Bladder cancer |
APOBEC3B was overexpressed in bladder cancer tissues |
Human tissue samples |
[8, 73] |
Lung cancer |
The APOBEC3B expression is elevated obviously in non-small cell lung cancer (NSCLC) tissues and the overexpression of APOBEC3B was correlated with unfavorable prognosis |
Human tissue samples |
[8, 74] |
The tumor/normal ratio of APOBEC3B mRNA levels was not different within the sexuality, age, smoking status, epidermal growth factor receptor (EGFR), kirsten rat sarcoma viral oncogene (KRAS) mutation and pathological stages |
Human tissue samples |
[75] |
Head and neck |
The mRNA level of APOBEC3B were significantly higher in cancer tissues than in the corresponding noncancerous esophageal mucosae |
Human tissue samples |
[8, 76] |
APOBEC3B mRNA expression was significantly higher in oral squamous cell carcinomas (OSCC), compared to non-cancerous oral tissues |
Human tissue samples |
[77] |
Ovarian cancer |
APOBEC3B may paly a potential role in serous ovarian cancer genomic instability |
Human tissue samples. In vitro, human cell lines |
[78] |