DIPG-01. LIN28B EXPRESSION IN DIFFUSE MIDLINE GLIOMA
نویسندگان
چکیده
Abstract INTRODUCTION Diffuse midline glioma (DMG) is the most lethal of all childhood cancers. LIN28B an RNA binding protein expressed in a variety cancers, which suppresses let-7 family microRNAs, turn plethora oncogenes. However, role DMG has not yet been explored. Therefore, we sought to determine pattern expression and potential function using rare cell lines. METHODS All studies were performed on lines (n=6) controls (normal human astrocytes n=1, neural stem cells n=1). RNA-Seq was single-read sequencing at 50bp Illumina NextSeq 500 Sequencing System. Cells then treated with DMSO or inhibitor, LI71, submitted functional vitro studies, as well Western Blot analysis. Functional pathways analysis subsequently resulting gene values Ingenuity Pathways Analysis (Qiagen). RESULTS Differential demonstrated across lines, expressing greater levels compared controls. inhibition small molecule inhibitor LI71 resulted decreased proliferation migration, vitro. A total 946 differentially genes identified between treatment groups (FC>2 <-2, p<0.05). implicated Cancer Neurological Disease top disease processes, Cellular Movement molecular process LIN28B. Further, inactivation Myc signaling LI71. CONCLUSIONS Our data demonstrates increased controls, oncogenic effects migration. Further investigation LIN28B-let7 axis warranted order further explore novel therapeutic target DMG.
منابع مشابه
A Protocol for Rapid Post-mortem Cell Culture of Diffuse Intrinsic Pontine Glioma (DIPG)
Diffuse Intrinsic Pontine Glioma (DIPG) is a childhood brainstem tumor that carries a universally fatal prognosis. Because surgical resection is not a viable treatment strategy and biopsy is not routinely performed, the availability of patient samples for research is limited. Consequently, efforts to study this disease have been challenged by a paucity of faithful disease models. To address thi...
متن کاملCirculatory YKL-40 & NLR: Underestimated Prognostic Indicators in Diffuse Glioma
In addition to histopathological parameters, evaluation of associated hematological factors is essential for devising a sensitive prognostic scale in glioma. Increased neutrophil-lymphocyte ratio (NLR), a marker of systemic inflammatory response, has recently been associated with worse outcome in various cancers. Given that glioma progression is characterized by inflammation, aggressive angioge...
متن کاملAbsence of MGMT promoter methylation in diffuse midline glioma, H3 K27M-mutant
Letter According to the revised 4th edition of the WHO classification of tumors of the CNS, diffuse midline gliomas, H3 K27M-mutant (DMG) are molecularly defined as tumors with a predominantly astrocytic differentiation carrying mutations in the histone H3 encoding genes H3F3A (histone H3.3), HIST1H3B (H3.1) or HIST1H3C (H3.2) [9]. The vast majority of DMG demonstrate typical features of gliobl...
متن کاملExtending the Neuroanatomic Territory of Diffuse Midline Glioma, K27M Mutant: Pineal Region Origin.
Diffuse midline glioma, H3-K27M mutant (DMG-K27M) is a newly described, molecularly distinct infiltrative glioma that almost exclusively arises in midline CNS structures, including the brain stem, especially the pons, as well as the thalamus and spinal cord with rare examples seen in the cerebellum, third ventricle, and hypothalamus. To our knowledge, only 1 case of a molecularly confirmed DMG-...
متن کاملDiffuse non-midline glioma with H3F3A K27M mutation: a prognostic and treatment dilemma
Recent studies have identified that K27M mutation in either the H3F3A or HIST1H3B genes, which encode the histone H3 variants H3.3 and H3.1, define the majority of diffuse gliomas arising in midline structures including the thalamus, brainstem, and spinal cord in both children and adults [8, 10]. These “diffuse midline gliomas, H3 K27M-mutant” are associated with poor prognosis regardless of hi...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Neuro-oncology
سال: 2023
ISSN: ['1523-5866', '1522-8517']
DOI: https://doi.org/10.1093/neuonc/noad073.048