DNA methylation levels of the ELMO gene promoter CpG islands in human glioblastomas
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DNA methylation levels of the ELMO gene promoter CpG islands in human glioblastomas. / Michaelsen, Signe Regner; Aslan, Derya; Urup, Thomas; Poulsen, Hans Skovgaard; Grønbæk, Kirsten; Broholm, Helle; Kristensen, Lasse Sommer.
I: International Journal of Molecular Sciences , Bind 19, Nr. 3, 679, 2018.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - DNA methylation levels of the ELMO gene promoter CpG islands in human glioblastomas
AU - Michaelsen, Signe Regner
AU - Aslan, Derya
AU - Urup, Thomas
AU - Poulsen, Hans Skovgaard
AU - Grønbæk, Kirsten
AU - Broholm, Helle
AU - Kristensen, Lasse Sommer
PY - 2018
Y1 - 2018
N2 - Complete surgical resection of glioblastoma is difficult due to the invasive nature of this primary brain tumor, for which the molecular mechanisms behind remain poorly understood. The three human ELMO genes play key roles in cellular motility, and have been linked to metastasis and poor prognosis in other cancer types. The aim of this study was to investigate methylation levels of the ELMO genes and their correlation to clinical characteristics and outcome in patients diagnosed with glioblastoma. To measure DNA methylation levels we designed pyrosequencing assays targeting the promoter CpG island of each the ELMO genes. These were applied to diagnostic tumor specimens from a well-characterized cohort of 121 patients who received standard treatment consisting of surgery, radiation therapy, plus concomitant and adjuvant chemotherapy. The promoter methylation levels of ELMO1 and ELMO2 were generally low, whereas ELMO3 methylation levels were high, in the tumor biopsies. Thirteen, six, and 18 biopsies were defined as aberrantly methylated for ELMO1, ELMO2, and ELMO3, respectively. There were no significant associations between the methylation status of any of the ELMO gene promoter CpG islands and overall survival, progression-free survival, and clinical characteristics of the patients including intracranial tumor location. Therefore, the methylation status of the ELMO gene promoter CpG islands is unlikely to have prognostic value in glioblastoma.
AB - Complete surgical resection of glioblastoma is difficult due to the invasive nature of this primary brain tumor, for which the molecular mechanisms behind remain poorly understood. The three human ELMO genes play key roles in cellular motility, and have been linked to metastasis and poor prognosis in other cancer types. The aim of this study was to investigate methylation levels of the ELMO genes and their correlation to clinical characteristics and outcome in patients diagnosed with glioblastoma. To measure DNA methylation levels we designed pyrosequencing assays targeting the promoter CpG island of each the ELMO genes. These were applied to diagnostic tumor specimens from a well-characterized cohort of 121 patients who received standard treatment consisting of surgery, radiation therapy, plus concomitant and adjuvant chemotherapy. The promoter methylation levels of ELMO1 and ELMO2 were generally low, whereas ELMO3 methylation levels were high, in the tumor biopsies. Thirteen, six, and 18 biopsies were defined as aberrantly methylated for ELMO1, ELMO2, and ELMO3, respectively. There were no significant associations between the methylation status of any of the ELMO gene promoter CpG islands and overall survival, progression-free survival, and clinical characteristics of the patients including intracranial tumor location. Therefore, the methylation status of the ELMO gene promoter CpG islands is unlikely to have prognostic value in glioblastoma.
KW - Clinical outcome
KW - DNA methylation
KW - ELMO1
KW - ELMO2
KW - ELMO3
KW - Glioblastoma
KW - Invasion
KW - Motility
U2 - 10.3390/ijms19030679
DO - 10.3390/ijms19030679
M3 - Journal article
C2 - 29495584
AN - SCOPUS:85042732185
VL - 19
JO - International Journal of Molecular Sciences (Online)
JF - International Journal of Molecular Sciences (Online)
SN - 1661-6596
IS - 3
M1 - 679
ER -
ID: 211864877