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Discovery of ERK5 inhibitors for biomarker-driven clinical evaluation in cancer

Discovery of ERK5 inhibitors for biomarker-driven clinical evaluation in cancer
发现 ERK5 抑制剂用于癌症生物标志物驱动的临床评估
批准号:
MR/K007580/1
负责人:
Herbie Newell
金额:
$106.06万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2013
资助国家:
英国
项目状态:
已结题
起止时间:
2013 至 --

项目摘要

项目成果

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中文摘要
翻译
癌症现在是英国最常见的疾病死亡原因,在所有发达国家也越来越普遍。在英国,前列腺癌是男性中最常见的恶性肿瘤,乳腺癌是女性中最常见的恶性肿瘤,在世界范围内,肝癌是第三大最常见的肿瘤类型。常见癌症的治疗选择仍然有限,只有药物治疗被证明对转移性疾病的管理有益,转移性疾病是癌症患者死亡的主要原因。尽管癌症治疗药物的范围和活性都在不断扩大,但在英国,每年仍有超过15万名患者死于癌症。因此,仍有大量未满足的临床需求,ERK5是一个令人兴奋的新药靶点,可用于多种肿瘤,包括前列腺癌、乳腺癌和肝癌。在为期2年的MRC DPFS奖期间,将开发信号酶ERK5的选择性和强效抑制剂,并确定临床试验候选化合物和备用化合物。随后,这些化合物将在癌症患者中进行评估,并明确新的癌症药物的临床开发途径。重要的是,ERK5抑制剂是新一代靶向癌症药物的代表,因此全面的测试或生物标志物组合对于候选药物的最佳临床前和临床开发以及它们最终作为分层药物的使用至关重要-即确保正确的患者在正确的时间获得正确的药物。这些生物标志物将与候选药物一起使用侵入性(活检)和非侵入性(成像)技术进行开发。该研究成果是一种新类别的新药,将为癌症患者提供令人兴奋的新治疗选择。此外,生物标志物的共同开发将使治疗针对那些最有可能受益的患者,并允许对ERK5抑制剂的治疗潜力进行早期评估。
英文摘要
Cancer is now the commonest cause of death from disease in the UK, and increasingly in all developed countries. In the UK, prostate cancer is the most common malignancy in males, breast cancer the most common in females and, worldwide, liver cancer is the 3rd most common tumour type. Therapeutic options for the common cancers remain limited, and only drug therapy is of proven benefit for the management of metastatic disease, the primary cause of death in cancer patients. Although the range and activity of drugs available for cancer treatment are improving, over 150,000 patients still die of the disease in the UK each year. Hence there remains a substantial unmet clinical need, and ERK5 is an exciting new drug target in multiple tumours including prostate, breast and liver cancer.Selective and potent inhibitors of the signalling enzyme ERK5 will be developed and a clinical trial candidate and a back-up compound identified during the 2 year MRC DPFS award. Subsequently, the compound(s) will be evaluated in patients with cancer and the clinical development pathway for new cancer medicines is well-defined. Importantly, ERK5 inhibitors are representative of the new generation of targeted cancer drugs and hence a comprehensive portfolio of tests or biomarkers is essential for the optimal pre-clinical and clinical development of drug candidates, and their eventual use as stratified medicines - i.e. making sure that the right patient gets the right drug at the right time. These biomarkers will be developed alongside the drug candidate using invasive (biopsy) and non-invasive (imaging) technologies.The research output, a new drug in a new class, will provide an exciting new treatment option for patients with cancer. Furthermore, the co-development of biomarkers will allow the treatment to be directed towards those patients who are most likely to benefit, and allow the early evaluation of the therapeutic potential of ERK5 inhibitors.
期刊论文(7)
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会议论文
DOI: 10.1021/acs.jmedchem.1c01756
发表时间: 2022-05-12
期刊: JOURNAL OF MEDICINAL CHEMISTRY
影响因子: 7.3
作者: [Miller, Duncan C., Reuillon, Tristan, Molyneux, Lauren, Blackburn, Timothy, Cook, Simon J., Edwards, Noel, Endicott, Jane A., Golding, Bernard T., Griffin, Roger J., Hardcastle, Ian, Harnor, Suzannah J., Heptinstall, Amy, Lochhead, Pamela, Martin, Mathew P., Martin, Nick C., Myers, Stephanie, Newell, David R., Noble, Richard A., Phillips, Nicole, Rigoreau, Laurent, Thomas, Huw, Tucker, Julie A., Wang, Lan-Zhen, Waring, Michael J., Wong, Ai-Ching, Wedge, Stephen R., Noble, Martin E. M., Cano, Celine]
通讯作者: Cano, Celine
DOI: 10.1021/acs.jmedchem.3c00072
发表时间: 2023-04-13
期刊: JOURNAL OF MEDICINAL CHEMISTRY
影响因子: 7.3
作者: [Miller, Duncan C., Harnor, Suzannah J., Martin, Mathew P., Noble, Richard A., Wedge, Stephen R., Cano, Celine]
通讯作者: Cano, Celine
DOI: 10.1080/15384101.2015.1120915
发表时间: 2016
期刊: Cell cycle (Georgetown, Tex.)
影响因子: --
作者: [Lochhead PA, Clark J, Wang LZ, Gilmour L, Squires M, Gilley R, Foxton C, Newell DR, Wedge SR, Cook SJ]
通讯作者: Cook SJ
MICA: Pre-clinical studies on a novel prodrug delivery technology for cystinosis.
  • 批准号:
    MR/P018254/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $201.41万
  • 财政年份:
    2018
  • 负责人:
    Herbie Newell
  • 依托单位:
MRC Contribution to a CR-UK and EPSRC Cancer Imaging Initiative
  • 批准号:
    MC_G0902167
  • 项目类别:
    Intramural
  • 资助金额:
    $382.26万
  • 财政年份:
    2008
  • 负责人:
    Herbie Newell
  • 依托单位:
FLIC - Functional Ligands for Imaging in Cancer
  • 批准号:
    EP/E000657/1
  • 项目类别:
    Research Grant
  • 资助金额:
    $53.3万
  • 财政年份:
    2006
  • 负责人:
    Herbie Newell
  • 依托单位:
国内基金
海外基金
姜黄素调控Oxtr/ERK5通路治疗子宫腺肌病疼痛的作用与机制研究
  • 批准号:
  • 项目类别:
    省市级项目
  • 资助金额:
    --
  • 批准年份:
    2025
  • 负责人:
    吴青
  • 依托单位:
ALKBH5去甲基化修饰调控慢性心衰LncRNA-miR143HG/ miRNA-143/ERK5通路的作用及温阳振衰颗粒的干预机制研究
ERK5抑制CD8+T细胞募集导致T790M突变晚期肺腺癌免疫检查点抑制剂耐药的机制研究
  • 批准号:
    82303749
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    30万元
  • 批准年份:
    2023
  • 负责人:
    赵文
  • 依托单位:
BMSCs源性外泌体水凝胶联合跑台运动通过细胞骨架-FAK/ERK5信号通路促进软骨缺损修复机制研究
  • 批准号:
  • 项目类别:
    省市级项目
  • 资助金额:
    10.0万元
  • 批准年份:
    2023
  • 负责人:
    宋锦旗
  • 依托单位: