Exploring Precision Oncology: From Gene Fusions to lncRNAs

探索精准肿瘤学：从基因融合到 lncRNA

• 批准号: 10462574
• 负责人: ARUL M CHINNAIYAN
• 金额: $ 91.01万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2018
• 资助国家: 美国
• 起止时间: 2018-09-01 至 2025-08-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10462574
• 关键词: Achievement; Advanced Malignant Neoplasm; Antisense Oligonucleotides; Area; Award; Biological; Biological Markers; Cancer Intervention; Cancer Patient; Clinical; Communities; Data; Development; Diagnosis; Diagnostic; Disseminated Malignant Neoplasm; ERG gene; Foundations; Gene Fusion; Goals; Human; Individual; Malignant Neoplasms; Malignant neoplasm of prostate; Mission; Modeling; Molecular; Molecular Target; PSA level; Pathogenesis; Patients; Peptides; Prognosis; Prostate; Reporting; Research; Research Personnel; Resources; Role; Sampling; Screening for Prostate Cancer; Serum; TMPRSS2 gene; Therapeutic Intervention; Untranslated RNA; Urine; Validation; Work; bioinformatics resource; cancer type; clinical sequencing; disease diagnosis; efficacious treatment; experience; inhibitor; knowledge base; novel marker; peptidomimetics; precision medicine; precision oncology; prognostic; programs; research clinical testing; single cell sequencing; targeted treatment; therapeutic development; therapeutic target; transcriptome; transcriptomics; translational cancer research; tumor progression

Project Summary / Abstract The potential of precision medicine to benefit the lives of cancer patients continues to emerge. The mission of the Chinnaiyan lab is to advance the field of precision oncology, and we aim to achieve this through the discovery and development of molecular targets that will aid in diagnosis, prognosis, or therapeutic intervention of cancers. Over the past several years, we have made a number of significant advancements in these areas. One of these landmark studies found that TMPRSS2-ETS gene fusions exist in the majority of prostate cancers. This discovery led to our development of a non-invasive clinical test (Mi-Prostate Score, MiPS) that combines analysis of urine levels of TMPRSS2-ERG and the long non-coding RNA (lncRNA) PCA3 with serum levels of PSA to detect prostate cancers. Due to its subsequently established roles in prostate cancer pathogenesis, we also reported on the development of peptidomimetic inhibitors (ERG inhibitory peptides, EIPs) of the ERG gene fusion product. A monumental achievement in the field of precision oncology has also been establishment of our comprehensive sequencing program for advanced cancer patients, called Mi-Oncoseq. Mi-Oncoseq has become a model for integrative clinical sequencing and generated several pivotal findings, including our recent report on the integrative sequencing analysis of metastatic cancers. Data from our sequencing program were also included in our report of the lncRNA landscape of the human transcriptome. Studies of individual lncRNAs have additionally emerged in our lab, such as validation of SChLAP1 as a marker for aggressive prostate cancer. This brief description of selected achievements highlights our commitment to advancing precision oncology and our vast foundational experience in this arena. Through the NCI Outstanding Investigator Award, we propose to continue these lines of research to further explore the diagnostic potential of precision oncology, therapeutic targeting of identified markers, and roles of nominated targets in cancer development. The future research program centered on diagnostic potential will include such initiatives as creation of new bioinformatic resources (e.g. “Mi-PANDA”, a compendia of transcriptomic data), high throughput single cell sequencing analysis of patient samples, and creation of cancer-specific lncRNA panels for use with non-invasive clinical isolates. Therapeutic targeting will be explored through the use of antisense oligos to lncRNAs and studies on the efficacy of peptidomimetics for gene fusions and “undruggable” targets. These avenues of research will provide impetus for studying the roles of selected noteworthy targets in cancer development. In particular, we have already discovered two lncRNAs, ARlnc1 and THOR1, which appear to be involved in cancer progression. Overall, this ambitious research program will advance the field of precision oncology by providing new community resources, identifying novel biomarkers, exploring the therapeutic targeting of nominated molecular players, and adding to the knowledge-base of cancer development mechanisms, particularly those of lncRNAs. Importantly, this award and the proposed work would assist our lab in its mission to remain a leader in the field of precision oncology.

项目概要/摘要 精准医学造福癌症患者生命的潜力不断显现。 Chinnaiyan 实验室致力于推进精准肿瘤学领域的发展，我们的目标是通过这一发现来实现这一目标 以及开发有助于癌症诊断、预后或治疗干预的分子靶点。 在过去的几年里，我们在这些领域取得了许多重大进展。 具有里程碑意义的研究发现，TMPRSS2-ETS基因融合体存在于大多数前列腺癌中。 导致我们开发了一种结合尿液分析的非侵入性临床测试（Mi-前列腺评分，MiPS） TMPRSS2-ERG和长链非编码RNA（lncRNA）PCA3的水平与血清​​PSA水平一起检测 由于其在前列腺癌发病机制中随后确定的作用，我们还报道了。 关于ERG基因融合产物的拟肽抑制剂（ERG抑制肽，EIPs）的开发。 我们在精准肿瘤学领域也取得了里程碑式的成就 名为 Mi-Oncoseq 的晚期癌症患者测序计划已成为一个模型。 综合临床测序并产生了一些关键发现，包括我们最近关于 我们的测序程序的数据也包含在转移性癌症的综合测序分析中。 我们对人类转录组 lncRNA 景观的报告还对单个 lncRNA 进行了研究。 我们实验室出现了一些新的技术，例如验证 SChLAP1 作为侵袭性前列腺癌的标志物。 对选定成就的简要描述突显了我们对推进精准肿瘤学和 通过 NCI 杰出研究者奖，我们建议： 继续这些研究方向，进一步探索精准肿瘤学、治疗学的诊断潜力 确定的标记物的靶向以及指定靶点在癌症发展中的作用。 以诊断潜力为中心的方案将包括创建新的生物信息资源等举措 （例如“Mi-PANDA”，转录组数据概要），高通量单细胞测序分析 患者样本，并创建癌症特异性 lncRNA 组合，用于非侵入性临床分离株。 将通过使用 lncRNA 反义寡核苷酸和功效研究来探索治疗靶向 用于基因融合和“不可成药”靶标的肽模拟物的研究将提供动力。 特别是，我们已经研究了选定的值得注意的靶点在癌症发展中的作用。 发现了两种 lncRNA，ARlnc1 和 THOR1，它们似乎与癌症进展有关。 雄心勃勃的研究计划将通过提供新的社区资源来推进精准肿瘤学领域， 识别新的生物标志物，探索指定分子参与者的治疗靶向，并添加 癌症发展机制的知识库，特别是 lncRNA 的知识库。 拟议的工作将有助于我们实验室履行其使命，保持精准肿瘤学领域的领导者地位。