Probing into low-density lipoprotein receptor-related protein (LPR)-1-independent peptide transcytosis mechanisms

低密度脂蛋白受体相关蛋白(LPR)-1独立肽转胞吞机制探讨

基本信息

  • 批准号:
    445033-2012
  • 负责人:
  • 金额:
    $ 6.34万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Collaborative Research and Development Grants
  • 财政年份:
    2015
  • 资助国家:
    加拿大
  • 起止时间:
    2015-01-01 至 2016-12-31
  • 项目状态:
    已结题

项目摘要

The Laboratory of Molecular Oncology at the Université du Québec à Montréal (UQAM) and under the direction of Professor Borhane Annabi is partnering with AngioChem a Montreal-based company reknown for its unique synthetic strategies applicable to breakthrough pharmacological agents that are optimized to cross the blood-brain barrier (BBB). Such technology will help to better understand molecular and cellular processes involved in central nervous system and brain-related disorders. The current project will investigate the molecular mechanisms involved in intracellular low-density lipoprotein receptor-related protein (LRP)-1 receptor-dependent and independent pathways. Such pathways open up a wide variety of original and sophisticated molecular strategies to explore new and original molecular and cellular processes involved in processes such as angiogenesis and impact of hypoxia (low oxygen levels) on cells and tissues. The current proposed collaborative project is designed to identify and investigate the alternate receptors and/or interacting molecular partners that could be involved in the transport of Angiopeps. This will result in an increased fundamental understanding of the LRP-1 transport mechanisms that will enable novel chemical entities to target critical cellular processes such as those involved in uncontrolled carcinogenic cell proliferation, cell survival, as well as those mechanisms involved in tumour-associated angiogenesis, and in brain-related disorders. The expected benefits will help to accrue to Canadian industry and to UQAM, the targeted areas under investigation in the described joint research and development activities are expected to leverage a breakthrough platform technology enabling physiological transport of bioactive molecules across the BBB. As such, AngioChem currently positions itself as the leader in this field. Academically, the direct benefits to UQAM include valuable training opportunities, increased employment as well as anchoring exciting industrial partnerships to the Montreal region. Scientifically, UQAM's Faculty of Sciences will enormously benefit of increased visibility from such an active partnership.
魁北克大学蒙特利尔分校(UQAM)的分子肿瘤学实验室在Borhane Annabi教授的指导下与AngioChem合作,AngioChem是一家总部位于蒙特利尔的公司,以其独特的合成策略而闻名,适用于突破性的药理学药物,这些药物经过优化可以穿过血脑屏障(BBB)。这种技术将有助于更好地了解中枢神经系统和脑相关疾病的分子和细胞过程。本课题主要研究细胞内低密度脂蛋白受体相关蛋白(LRP)-1受体依赖性和非依赖性通路的分子机制。这些途径开辟了各种各样的原始和复杂的分子策略,以探索参与诸如血管生成和缺氧(低氧水平)对细胞和组织的影响等过程的新的和原始的分子和细胞过程。目前提出的合作项目旨在确定和研究可能参与血管肽转运的替代受体和/或相互作用的分子伴侣。这将导致对LRP-1转运机制的基本理解增加,这将使新的化学实体能够靶向关键的细胞过程,例如参与不受控制的致癌细胞增殖、细胞存活的那些过程,以及参与肿瘤相关血管生成和脑相关疾病的那些机制。预期的好处将有助于加拿大工业和UQAM,在所述联合研发活动中调查的目标领域预计将利用突破性平台技术,使生物活性分子能够通过BBB进行生理运输。因此,AngioChem目前将自己定位为该领域的领导者。在学术上,UQAM的直接好处包括宝贵的培训机会,增加就业机会以及将令人兴奋的工业伙伴关系锚定到蒙特利尔地区。科学家们,UQAM的科学学院将极大地受益于这种积极的合作伙伴关系提高知名度。

项目成果

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Annabi, Borhane其他文献

Cell-based evidence for aminopeptidase N/CD13 inhibitor actinonin targeting of MT1-MMP-mediated proMMP-2 activation
  • DOI:
    10.1016/j.canlet.2009.01.032
  • 发表时间:
    2009-07-08
  • 期刊:
  • 影响因子:
    9.7
  • 作者:
    Sina, Asmaa;Lord-Dufour, Simon;Annabi, Borhane
  • 通讯作者:
    Annabi, Borhane
Pharmacological targeting of β-adrenergic receptor functions abrogates NF-κB signaling and MMP-9 secretion in medulloblastoma cells
  • DOI:
    10.2147/ott.s14503
  • 发表时间:
    2010-01-01
  • 期刊:
  • 影响因子:
    4
  • 作者:
    Annabi, Borhane;Vaillancourt-Jean, Eric;Beliveau, Richard
  • 通讯作者:
    Beliveau, Richard
Antiproliferative efficacy of elderberries and elderflowers (Sambucus canadensis) on glioma and brain endothelial cells under normoxic and hypoxic conditions
  • DOI:
    10.1016/j.jff.2017.10.048
  • 发表时间:
    2018-01-01
  • 期刊:
  • 影响因子:
    5.6
  • 作者:
    Lamy, Sylvie;Muhire, Evelyne;Annabi, Borhane
  • 通讯作者:
    Annabi, Borhane
The Peptide-Drug Conjugate TH1902: A New Sortilin Receptor-Mediated Cancer Therapeutic against Ovarian and Endometrial Cancers.
  • DOI:
    10.3390/cancers14081877
  • 发表时间:
    2022-04-08
  • 期刊:
  • 影响因子:
    5.2
  • 作者:
    Currie, Jean-Christophe;Demeule, Michel;Charfi, Cyndia;Zgheib, Alain;Larocque, Alain;Danalache, Bogdan Alexandru;Ouanouki, Amira;Beliveau, Richard;Marsolais, Christian;Annabi, Borhane
  • 通讯作者:
    Annabi, Borhane
Silencing of the MT1-MMP/G6PT axis suppresses calcium mobilization by sphingosine-1-phosphate in glioblastoma cells
  • DOI:
    10.1016/j.febslet.2008.01.061
  • 发表时间:
    2008-03-05
  • 期刊:
  • 影响因子:
    3.5
  • 作者:
    Fortier, Simon;Labelle, Dominique;Annabi, Borhane
  • 通讯作者:
    Annabi, Borhane

Annabi, Borhane的其他文献

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{{ truncateString('Annabi, Borhane', 18)}}的其他基金

Probing into receptor-mediated trafficking and internalization functions of biologically active peptides
生物活性肽受体介导的运输和内化功能的探讨
  • 批准号:
    RGPIN-2018-06651
  • 财政年份:
    2022
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual
Probing into receptor-mediated trafficking and internalization functions of biologically active peptides
生物活性肽受体介导的运输和内化功能的探讨
  • 批准号:
    RGPIN-2018-06651
  • 财政年份:
    2021
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual
Probing into receptor-mediated trafficking and internalization functions of biologically active peptides
生物活性肽受体介导的运输和内化功能的探讨
  • 批准号:
    RGPIN-2018-06651
  • 财政年份:
    2020
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual
Probing into receptor-mediated trafficking and internalization functions of biologically active peptides
生物活性肽受体介导的运输和内化功能的探讨
  • 批准号:
    RGPIN-2018-06651
  • 财政年份:
    2019
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual
Probing into receptor-mediated trafficking and internalization functions of biologically active peptides
生物活性肽受体介导的运输和内化功能的探讨
  • 批准号:
    RGPIN-2018-06651
  • 财政年份:
    2018
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual
Probing into low-density lipoprotein receptor-related protein (LPR)-1-independent peptide transcytosis mechanisms
低密度脂蛋白受体相关蛋白(LPR)-1独立肽转胞吞机制探讨
  • 批准号:
    445033-2012
  • 财政年份:
    2014
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Collaborative Research and Development Grants
Metabolic and tumorigenic adaptation in mesenchymal stromal cells : a new bioswitch function for the glucose-6-phosphate translocase
间充质基质细胞的代谢和致瘤适应:葡萄糖-6-磷酸转位酶的新生物开关功能
  • 批准号:
    288249-2010
  • 财政年份:
    2014
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual
Metabolic and tumorigenic adaptation in mesenchymal stromal cells : a new bioswitch function for the glucose-6-phosphate translocase
间充质基质细胞的代谢和致瘤适应:葡萄糖-6-磷酸转位酶的新生物开关功能
  • 批准号:
    288249-2010
  • 财政年份:
    2013
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual
Probing into low-density lipoprotein receptor-related protein (LPR)-1-independent peptide transcytosis mechanisms
低密度脂蛋白受体相关蛋白(LPR)-1独立肽转胞吞机制探讨
  • 批准号:
    445033-2012
  • 财政年份:
    2013
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Collaborative Research and Development Grants
Metabolic and tumorigenic adaptation in mesenchymal stromal cells : a new bioswitch function for the glucose-6-phosphate translocase
间充质基质细胞的代谢和致瘤适应:葡萄糖-6-磷酸转位酶的新生物开关功能
  • 批准号:
    288249-2010
  • 财政年份:
    2012
  • 资助金额:
    $ 6.34万
  • 项目类别:
    Discovery Grants Program - Individual

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