دورية أكاديمية

Altered expression of stromal interaction molecule (STIM)-calcium release-activated calcium channel protein (ORAI) and inositol 1,4,5-trisphosphate receptors (IP3Rs) in cancer: will they become a new battlefield for oncotherapy?

التفاصيل البيبلوغرافية
العنوان: Altered expression of stromal interaction molecule (STIM)-calcium release-activated calcium channel protein (ORAI) and inositol 1,4,5-trisphosphate receptors (IP3Rs) in cancer: will they become a new battlefield for oncotherapy?
المؤلفون: Jing Wen, Ying-Cheng Huang, Huan-Huan Xiu, Zhi-Ming Shan, Kang-Qing Xu
المصدر: Chinese Journal of Cancer, Vol 35, Iss 1, Pp 1-9 (2016)
بيانات النشر: BMC, 2016.
سنة النشر: 2016
المجموعة: LCC:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
مصطلحات موضوعية: Stromal interaction molecule (STIM), Calcium release-activated calcium channel protein (ORAI), Inositol 1,4,5-trisphosphate receptors (IP3Rs), Ca2+, Tumorigenesis, Neoplasms. Tumors. Oncology. Including cancer and carcinogens, RC254-282
الوصف: Abstract The stromal interaction molecule (STIM)-calcium release-activated calcium channel protein (ORAI) and inositol 1,4,5-trisphosphate receptors (IP3Rs) play pivotal roles in the modulation of Ca2+-regulated pathways from gene transcription to cell apoptosis by driving calcium-dependent signaling processes. Increasing evidence has implicated the dysregulation of STIM–ORAI and IP3Rs in tumorigenesis and tumor progression. By controlling the activities, structure, and/or expression levels of these Ca2+-transporting proteins, malignant cancer cells can hijack them to drive essential biological functions for tumor development. However, the molecular mechanisms underlying the participation of STIM–ORAI and IP3Rs in the biological behavior of cancer remain elusive. In this review, we summarize recent advances regarding STIM–ORAI and IP3Rs and discuss how they promote cell proliferation, apoptosis evasion, and cell migration through temporal and spatial rearrangements in certain types of malignant cells. An understanding of the essential roles of STIM–ORAI and IP3Rs may provide new pharmacologic targets that achieve a better therapeutic effect by inhibiting their actions in key intracellular signaling pathways.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1944-446X
Relation: http://link.springer.com/article/10.1186/s40880-016-0094-2; https://doaj.org/toc/1944-446X
DOI: 10.1186/s40880-016-0094-2
URL الوصول: https://doaj.org/article/33325a0ebb844a2699e988c64a3b82ca
رقم الأكسشن: edsdoj.33325a0ebb844a2699e988c64a3b82ca
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1944446X
DOI:10.1186/s40880-016-0094-2