Validation

Gene Symbol Curated Descriptions Cell Lines Isolationssort descending Validations Control-case Tumor Stage & Subtype Clinical Use PMID
EPCAM Tumour-derived exosomes interfere with the tumour-specific function of immune cells and constitute an additional mechanism how tumours escape from immune surveillance BT474 ultracentrifugation electron microscopy 21293856
ERBB2 Tumour-derived exosomes interfere with the tumour-specific function of immune cells and constitute an additional mechanism how tumours escape from immune surveillance BT474 ultracentrifugation electron microscopy 21293856
FGFR2 Presumably aid in targeting the primary cancer cells to specific metastatic sites 4T1 ultracentrifugation transmission electron microscopy metastasis 29115712
FGFR3 Presumably aid in targeting the primary cancer cells to specific metastatic sites 4T1 ultracentrifugation transmission electron microscopy metastasis 29115712
FIBP Presumably aid in targeting the primary cancer cells to specific metastatic sites 4T1 ultracentrifugation transmission electron microscopy metastasis 29115712
FRS2 Presumably aid in targeting the primary cancer cells to specific metastatic sites 4T1 ultracentrifugation transmission electron microscopy metastasis 29115712
GSTP1 Affecting drug metabolism---Anthracycline/taxane-based neoadjuvant chemotherapy MCF7 ultracentrifugation transmission electron microscopy drug resistance 28438694
hsa-miR-100 Target gene prediction and pathway analysis showed the involvement of miR-100, miR-222, and miR-30a in pathways implicated in cancer pathogenesis, membrane vesiculation and therapy failure，the transmition of chemoresistance by a horizontal transfer of miRNAs MCF7 ultracentrifugation transmission electron microscopy drug resistance 24740415
hsa-miR-105 Hsa-miR-105 has significantly up-regulated and has been extensively implicated in cancer progression MDA-MB-231 ultracentrifugation electron microscopy metastasis 24735924
hsa-miR-106b The mir-106b is found in higher levels in MCF-Eox as well, which can promote breast cancer invasion and metastasis by targeting BRMS1 and RB MCF7,MDA-MB231 ultracentrifugation electron microscopy 24468161

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