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GENE:

XAGE1A (X Antigen Family Member 1A)

i
Other names: XAGE1A, X Antigen Family Member 1A, XAGE-1, Cancer/Testis Antigen Family 12, Member 1a, G Antigen Family D Member 2, Cancer/Testis Antigen 12.1, X Antigen Family Member 1, G Antigen, Family D, 2, CT12.1, GAGED2, XAGE1, Cancer/Testis Antigen Family 12, Member 1b, Cancer/Testis Associated Protein, X Antigen Family, Member 1A, X Antigen Family, Member 1, X Antigen Family Member 1B, Protein XAGE-1, CT12.1A, CT12.1B, CT12.1a, XAGE1B, XAGE1A, XAGE1C, XAGE1D, XAGE1E, CTP9
4ms
Cancer-testis antigens (CTAs) in lung cancer. (PubMed, Clin Chim Acta)
We also discuss the incorporation of CTA testing in lung cancer diagnostic workflows with focus on its analytical performance, preanalytical factors as well as comparative value vs existing markers. Finally, we outline the role of CTAs as companion diagnostics in immunotherapy and targeted treatment plans, and indicate the main challenges and research priorities towards the clinical translation of CTAs.
Review • Journal • IO Companion diagnostic • IO biomarker
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CTAG1B (Cancer/testis antigen 1B) • XAGE1A (X Antigen Family Member 1A) • SPAG9 (Sperm Associated Antigen 9)
over3years
Serum Biomarker Panel for Rapid Early Diagnosis of Lung Cancer. (PubMed, Curr Cancer Drug Targets)
IL2RB, CENPB, TP53, and XAGE1A combined biomarker panel holds potential for rapid screening and could improve the diagnosis of early-stage LC, thus potentially also improving its prognosis.
Journal
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TP53 (Tumor protein P53) • XAGE1A (X Antigen Family Member 1A)
4years
Cancer testis antigen XAGE-1 is a promising marker for the diagnosis and treatment of ovarian cancer. (PubMed, J Med Life)
The connection of high XAGE 1 level with advanced ovarian cancer stages has also been established, supporting XAGE 1's proposed role in poor prognosis. Finally, finding the specific involvement of this gene in ovarian cancer and other kinds of malignancies may require further investigations.
Journal • IO biomarker
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XAGE1A (X Antigen Family Member 1A)
over4years
Measurable residual disease monitoring of SPAG6, ST18, PRAME, and XAGE1A expression in peripheral blood may detect imminent relapse in childhood acute myeloid leukemia. (PubMed, J Mol Diagn)
Only 1/130 (0.8%) follow-up analyses performed in 10 patients in continuous complete remission had transient expression above normal. Monitoring of SPAG6, ST18, PRAME, and XAGE1A expression in PB may predict relapse in childhood AML patients and facilitate molecular MRD monitoring in the majority of patients without a leukemia-specific target.
Clinical • Journal
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MSLN (Mesothelin) • PRAME (Preferentially Expressed Antigen In Melanoma) • XAGE1A (X Antigen Family Member 1A)