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Research Articles

A bioinformatics analysis of the clinicopathological and prognostic significance of FAM64A mRNA expression in gynecological cancers

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Article: 2216280 | Received 31 Mar 2023, Accepted 16 May 2023, Published online: 25 May 2023

Figures & data

Figure 1. The clinicopathological and prognostic significance of FAM64A mRNA expression in breast cancer. According to xiantao (A), UALCAN (B), GEO (C), and TCGA (D) databases, FAM64A overexpression was detectable in breast cancer when compared with normal breast tissue (p < 0.05). FAM64A expression was compared with breast cancer clinicopathological characteristics in UALCAN (E). In the Kaplan-Meier plotter (F), relationships between FAM64A expression and breast cancer patients were analysed and stratified by clinicopathological features. Note: N, normal tissue; T, tumour; HR, hazard ratio; ** p < 0.01; *** p < 0.001.

Figure 1. The clinicopathological and prognostic significance of FAM64A mRNA expression in breast cancer. According to xiantao (A), UALCAN (B), GEO (C), and TCGA (D) databases, FAM64A overexpression was detectable in breast cancer when compared with normal breast tissue (p < 0.05). FAM64A expression was compared with breast cancer clinicopathological characteristics in UALCAN (E). In the Kaplan-Meier plotter (F), relationships between FAM64A expression and breast cancer patients were analysed and stratified by clinicopathological features. Note: N, normal tissue; T, tumour; HR, hazard ratio; ** p < 0.01; *** p < 0.001.

Table 1. Relationships between FAM64A mRNA expression and breast cancer clinicopathological characteristics using the xiantao database.

Table 2. Overall survival analysis in breast cancer patients using the xiantao database.

Table 3. Disease-specific survival analysis of breast cancer patients using the xiantao database.

Figure 2. The clinicopathological and prognostic significance of FAM64A mRNA expression in cervical cancer. According to xiantao (A), UALCAN (B), TCGA (C), and GEO (D) databases, FAM64A hyperexpression was detectable in cervical cancer when compared with normal cervical tissue (p < 0.05). In the Kaplan-Meier plotter (E), relationships between FAM64A expression and cervical cancer patient survival data were analysed and stratified by clinicopathological features. Note: N, normal tissue; T, tumour; HR, hazard ratio; ***p < 0.001.

Figure 2. The clinicopathological and prognostic significance of FAM64A mRNA expression in cervical cancer. According to xiantao (A), UALCAN (B), TCGA (C), and GEO (D) databases, FAM64A hyperexpression was detectable in cervical cancer when compared with normal cervical tissue (p < 0.05). In the Kaplan-Meier plotter (E), relationships between FAM64A expression and cervical cancer patient survival data were analysed and stratified by clinicopathological features. Note: N, normal tissue; T, tumour; HR, hazard ratio; ***p < 0.001.

Figure 3. The clinicopathological and prognostic significance of FAM64A mRNA expression in endometrial cancer. According to xiantao (A), UALCAN (B), and TCGA (C) databases, FAM64A hyperexpression was detectable in endometrial cancer when compared with normal endometrial tissue (p < 0.05). FAM64A expression was compared with endometrial cancer clinicopathological characteristics in UALCAN (D). In the Kaplan-Meier plotter (E), relationships between FAM64A expression and endometrial cancer patient survival data were analysed and stratified by clinicopathological features. Note: N, normal tissue; T, tumour; HR, hazard ratio; **p < 0.01; ***p < 0.001.

Figure 3. The clinicopathological and prognostic significance of FAM64A mRNA expression in endometrial cancer. According to xiantao (A), UALCAN (B), and TCGA (C) databases, FAM64A hyperexpression was detectable in endometrial cancer when compared with normal endometrial tissue (p < 0.05). FAM64A expression was compared with endometrial cancer clinicopathological characteristics in UALCAN (D). In the Kaplan-Meier plotter (E), relationships between FAM64A expression and endometrial cancer patient survival data were analysed and stratified by clinicopathological features. Note: N, normal tissue; T, tumour; HR, hazard ratio; **p < 0.01; ***p < 0.001.
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Data availability statement

The datasets in this study can be found in online repositories. The names and accession numbers of the repository/repositories can be found in the article/Supplementary Materials.