22. DISCUSSION
AUTHOR
Penalva et al. 2000;
Small et al. 2006
WTAP is a highly conserved protein that partners
with WT1 to function as a switch gene, regulating
the balance between quiescence and proliferation.
Diaz-Miqueli and Martinez
2013
In the past decades, despite the recognized
treatment for patients with gliomas is surgery
followed by chemotherapy and radiotherapy,
especially for the patients with high-grade gliomas,
therapeutic failure and disease progression are still
quite frequent
23. DISCUSSION
AUTHOR
Jin et al. 2012; Small et al.
2007
Du-Il Jin found that WTAP expression was greater
in GBM than in normal brain tissues and WTAP
could regulate proliferation, migration, and invasion
of GBM cell lines.
Finkel et al. 2007; Music et al.
2016; Yang et al. 2015; Zeng et
al.2016.
In other prognostic research, age and glioma grade
were demonstrated to be an independent
prognostic factor and as it is known that the
in-cidence rates increases with age for most
cancers including gliomas.
24. *A correlation between expression WTAP and patient survival is evident, in this case WTAP is a negative
prognostic factor. Increasing WTAP is associated with decreased survival of patients.
*Mortality in gliomas leads to the investigation of methods for tumor diagnosis and prognosis based on
biomarkers to develop better treatment and early diagnosis. WTAP expression in glioma indicate that it
could serve as a new prognostic marker and provide more options to improve treatment.
*Overexpression of WTAP is closely related with glioma grade.
*WTAP expression, age, glioma grade and ECOG are associated with survival of patients.
CONCLUSION
25.
26.
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September 2016].
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September 2016].
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http://www.abta.org/brain-tumor-information/types-of-tumors/glioma.html?referrer=https://www.google.com.co/[Accessed 12
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6.
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