Academic Journal

The PTEN Tumor Suppressor Gene in Soft Tissue Sarcoma

التفاصيل البيبلوغرافية
العنوان: The PTEN Tumor Suppressor Gene in Soft Tissue Sarcoma
المؤلفون: Sioletic Stefano, Scambia Giovanni
المصدر: Cancers; Volume 11; Issue 8; Pages: 1169
بيانات النشر: Multidisciplinary Digital Publishing Institute
سنة النشر: 2019
المجموعة: MDPI Open Access Publishing
مصطلحات موضوعية: PTEN, Soft tissue sarcoma, liposarcoma, leiomyosarcoma, malignant peripheral nerve sheath tumor, undifferentiated pleomorphic sarcoma, myxofibrosarcoma, gastrointestinal stromal tumor, epithelioid sarcoma, synovial sarcoma
الوصف: Soft tissue sarcoma (STS) is a rare malignancy of mesenchymal origin classified into more than 50 different subtypes with distinct clinical and pathologic features. Despite the poor prognosis in the majority of patients, only modest improvements in treatment strategies have been achieved, largely due to the rarity and heterogeneity of these tumors. Therefore, the discovery of new prognostic and predictive biomarkers, together with new therapeutic targets, is of enormous interest. Phosphatase and tensin homolog (PTEN) is a well-known tumor suppressor that commonly loses its function via mutation, deletion, transcriptional silencing, or protein instability, and is frequently downregulated in distinct sarcoma subtypes. The loss of PTEN function has consequent alterations in important pathways implicated in cell proliferation, survival, migration, and genomic stability. PTEN can also interact with other tumor suppressors and oncogenic signaling pathways that have important implications for the pathogenesis in certain STSs. The aim of the present review is to summarize the biological significance of PTEN in STS and its potential role in the development of new therapeutic strategies.
نوع الوثيقة: text
وصف الملف: application/pdf
اللغة: English
Relation: https://dx.doi.org/10.3390/cancers11081169
DOI: 10.3390/cancers11081169
الاتاحة: https://doi.org/10.3390/cancers11081169
Rights: https://creativecommons.org/licenses/by/4.0/
رقم الانضمام: edsbas.437BCE7D
قاعدة البيانات: BASE