Stem cells' guided gene therapy of cancer: New frontier in personalized and targeted therapy.

Maria Mavroudi, Paul Zarogoulidis, Konstantinos Porpodis, Ioannis Kioumis, Sofia Lampaki, Lonny Yarmus, Raf Malecki, Konstantinos Zarogoulidis, Marek Malecki
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引用次数: 0

Abstract

Introduction: Diagnosis and therapy of cancer remain to be the greatest challenges for all physicians working in clinical oncology and molecular medicine. The statistics speak for themselves with the grim reports of 1,638,910 men and women diagnosed with cancer and nearly 577,190 patients passed away due to cancer in the USA in 2012. For practicing clinicians, who treat patients suffering from advanced cancers with contemporary systemic therapies, the main challenge is to attain therapeutic efficacy, while minimizing side effects. Unfortunately, all contemporary systemic therapies cause side effects. In treated patients, these side effects may range from nausea to damaged tissues. In cancer survivors, the iatrogenic outcomes of systemic therapies may include genomic mutations and their consequences. Therefore, there is an urgent need for personalized and targeted therapies. Recently, we reviewed the current status of suicide gene therapy for cancer. Herein, we discuss the novel strategy: genetically engineered stem cells' guided gene therapy.

Review of therapeutic strategies in preclinical and clinical trials: Stem cells have the unique potential for self renewal and differentiation. This potential is the primary reason for introducing them into medicine to regenerate injured or degenerated organs, as well as to rejuvenate aging tissues. Recent advances in genetic engineering and stem cell research have created the foundations for genetic engineering of stem cells as the vectors for delivery of therapeutic transgenes. Specifically in oncology, the stem cells are genetically engineered to deliver the cell suicide inducing genes selectively to the cancer cells only. Expression of the transgenes kills the cancer cells, while leaving healthy cells unaffected. Herein, we present various strategies to bioengineer suicide inducing genes and stem cell vectors. Moreover, we review results of the main preclinical studies and clinical trials. However, the main risk for therapeutic use of stem cells is their cancerous transformation. Therefore, we discuss various strategies to safeguard stem cell guided gene therapy against iatrogenic cancerogenesis.

Perspectives: Defining cancer biomarkers to facilitate early diagnosis, elucidating cancer genomics and proteomics with modern tools of next generation sequencing, and analyzing patients' gene expression profiles provide essential data to elucidate molecular dynamics of cancer and to consider them for crafting pharmacogenomics-based personalized therapies. Streamlining of these data into genetic engineering of stem cells facilitates their use as the vectors delivering therapeutic genes into specific cancer cells. In this realm, stem cells guided gene therapy becomes a promising new frontier in personalized and targeted therapy of cancer.

Abstract Image

干细胞引导的癌症基因治疗:个体化和靶向治疗的新前沿。
癌症的诊断和治疗仍然是所有临床肿瘤学和分子医学医生面临的最大挑战。2012年,美国有1,638,910名男性和女性被诊断患有癌症,近577,190名患者因癌症去世,这些统计数据不言自明。对于用现代系统疗法治疗晚期癌症患者的临床医生来说,主要的挑战是在达到治疗效果的同时尽量减少副作用。不幸的是,所有的现代全身疗法都有副作用。在接受治疗的患者中,这些副作用可能从恶心到组织受损。在癌症幸存者中,全身治疗的医源性结果可能包括基因组突变及其后果。因此,迫切需要个性化和靶向治疗。最近,我们回顾了自杀基因治疗癌症的现状。在此,我们讨论新的策略:基因工程干细胞引导基因治疗。临床前和临床试验治疗策略综述:干细胞具有自我更新和分化的独特潜力。这种潜力是将它们引入医学以再生受伤或退化的器官以及使衰老组织恢复活力的主要原因。基因工程和干细胞研究的最新进展为干细胞作为治疗性转基因载体的基因工程创造了基础。特别是在肿瘤学中,干细胞经过基因工程改造,只选择性地将细胞自杀诱导基因传递给癌细胞。转基因的表达杀死癌细胞,而不影响健康细胞。在此,我们提出了多种生物工程自杀诱导基因和干细胞载体的策略。此外,我们回顾了主要的临床前研究和临床试验的结果。然而,干细胞用于治疗的主要风险是它们的癌变。因此,我们讨论各种策略,以保障干细胞引导的基因治疗对医源性癌症的发生。观点:定义癌症生物标志物以促进早期诊断,利用下一代测序的现代工具阐明癌症基因组学和蛋白质组学,以及分析患者基因表达谱,为阐明癌症的分子动力学提供了必要的数据,并为制定基于药物基因组学的个性化治疗提供了考虑。将这些数据简化为干细胞的基因工程,有助于它们作为载体将治疗基因传递到特定的癌细胞中。在这一领域,干细胞引导的基因治疗成为癌症个性化和靶向治疗的一个有前景的新领域。
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