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. 2023 Jan 12;11(1):200. doi: 10.3390/biomedicines11010200

Table 3.

The implication of the differentially expressed genes by young age ER-positive breast cancer in tumorigenesis and cancer progression.

Gene ID Expression Status in Young-Age Breast Cancer Fold Change FDR p-Value Significance from Previous Literature References
DPYSL2 Up-regulated 4.25 0.0099 DYYSL2 is a regulator of cytoskeletal dynamics in growing axons. DPYSL2 knockout in mesenchymal-like cells inhibits cell migration, invasion, stemness features, tumour growth rate, and metastasis. Interaction between DPYSL2 and Janus kinase 1 induces the expression of vimentin which is a marker for epithelial-mesenchymal transition (EMT) and involved in cancer progression. [22]
MUCL1 Up-regulated 448.69 0.0099 Higher expression of MUCL1 was observed in HER2-amplified breast tumors. MUCL1 plays an essential role for MUCL1 in the proliferation of breast cancer cells, through the FAK/JNK signaling pathway. [23]
SFXN2 Down-regulated −4.76 0.0247 Loss of SFXN2 resulted in the accumulation of mitochondrial iron, and increased mitochondrial iron levels in TNBC generated large amounts of ROS that activated the NF-κB and TGF-β signaling pathways, which eventually promoted cell migration. [24]
GSN Up-regulated 3.32 0.0247 Higher expression of gelsolin was reported to be associated with axillary lymph node metastasis. [25]
RANBP3L Down-regulated 14.28 0.0277 In murine renal cells, loss of Ranbp3L expression resulted in the loss of epithelial characteristics, enhanced migration behavior and colony-forming capacity, and substantially altered gene expression profiles. [26,27]
ESR1 Down-regulated −22.62 0.0247 In estrogen receptor-positive breast cancer, a low level of ESR1 mRNA expression was a determinant of tamoxifen resistance in both adjuvant treatment and prevention settings. [28]
ACVR2A Up-regulated 4.65 0.0259 Over-expression of ACVR2A was associated with larger tumors (T3 and T4) in colorectal cancer clinical samples. This indicates an association between ACVR2A expression and the tumor growth process. [29]
GLYATL1 Down-regulated −21.37 0.0332 Down-regulated in several cancers and loss of expression was associated with higher tumor grade and poor prognosis in prostate adenocarcinoma and hepatocellular carcinoma patients. [30,31]
TSHZ2 Up-regulated 8.44 0.0332 Up-regulation of TSHZ2 was found to repress tumor growth and metastasis and induce mammary gland development in mice. [32]
SERPINE2 Up-regulated 9.27 0.0497 SerpinE2 overexpression in breast cancer was shown to promote metastatic spread by modulating the extracellular matrix. [33]
WDFY1 Up-regulated 2.52 0.0497 WDFY1 positively regulated Toll-like receptor (TLR) 3 and 4 signalings. TLR signaling regulates breast cancer cell proliferation in TP53 mutated cells. [34]
PCDHGB7 Up-regulated 3.63 0.0497 Overexpression of PCDH7 stimulated breast cancer cell proliferation and invasion in vitro and the formation of bone metastasis in vivo. PCDH7 was found to play role in bone metastasis in breast cancer. [35]