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Original Research

Characterization of AKT Somatic Mutations in Chinese Breast Cancer Patients

, , , , , , , , , ORCID Icon, ORCID Icon, , , ORCID Icon, , ORCID Icon, ORCID Icon, & show all
Pages 3055-3065 | Published online: 07 Apr 2021

Figures & data

Table 1 Clinicopathological Features of Breast Cancer Patients in GDPH and TCGA Databases

Figure 1 The mutation rates of AKT, AKT1, AKT2, and AKT3 in GDPH and TCGA cohorts of patients with breast cancer.

Abbreviations: GDPH, Guangdong Provincial People’s Hospital; TCGA, The Cancer Genome Atlas.
Figure 1 The mutation rates of AKT, AKT1, AKT2, and AKT3 in GDPH and TCGA cohorts of patients with breast cancer.

Figure 2 The frequency of different mutation types of (A) AKT, (B) AKT1, AKT2, and AKT3 in the two cohorts.

Abbreviations: GDPH, Guangdong Provincial People’s Hospital; TCGA, The Cancer Genome Atlas; AMP, copy number amplification; HOMDEL, homozygous deletions.
Figure 2 The frequency of different mutation types of (A) AKT, (B) AKT1, AKT2, and AKT3 in the two cohorts.

Figure 3 Diagram of domains of (A) AKT1, (B) AKT2 and (C) AKT3 with mutations identified in the GDPH cohort.

Abbreviation: PH, pleckstrin homology.
Figure 3 Diagram of domains of (A) AKT1, (B) AKT2 and (C) AKT3 with mutations identified in the GDPH cohort.

Table 2 Correlation Between Clinicopathological Features and AKT Family Mutation in GDPH and TCGA Databases

Table 3 AKT Inhibitors in Clinical Development