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Treatment of non-muscle invasive bladder cancer with Bacillus Calmette–Guerin (BCG): Biological markers and simulation studies

机译:卡介苗芽孢杆菌(BCG)治疗非肌肉浸润性膀胱癌:生物学标记和模拟研究

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Intravesical Bacillus Calmette–Guerin (BCG) vaccine is the preferred first line treatment for non-muscle invasive bladder carcinoma (NMIBC) in order to prevent recurrence and progression of cancer. There is ongoing need for the rational selection of i) {BCG} dose, ii) frequency of {BCG} administration along with iii) synergistic adjuvant therapy and iv) a reliable set of biochemical markers relevant to tumor response. In this review we evaluate cellular and molecular markers pertinent to the immunological response triggered by the {BCG} instillation and respective mathematical models of the treatment. Specific examples of markers include diverse immune cells, genetic polymorphisms, miRNAs, epigenetics, immunohistochemistry and molecular biology ‘beacons’ as exemplified by cell surface proteins, cytokines, signaling proteins and enzymes. We identified tumor associated macrophages (TAMs), human leukocyte antigen (HLA) class I, a combination of Ki-67/CK20, IL-2, IL-8 and IL-6/IL-10 ratio as the most promising markers for both pre-BCG and post-BCG treatment suitable for the simulation studies. The intricate and patient-specific nature of these data warrants the use of powerful multi-parametral mathematical methods in combination with molecular/cellular biology insight and clinical input.
机译:膀胱内卡介苗芽孢杆菌(BCG)疫苗是非肌肉浸润性膀胱癌(NMIBC)的首选一线治疗,以防止癌症的复发和发展。一直需要合理选择i){BCG}剂量,ii){BCG}给药频率以及iii)协同辅助治疗和iv)与肿瘤反应有关的可靠的生化标志物。在这篇综述中,我们评估了与{BCG}滴注引发的免疫反应有关的细胞和分子标志物以及治疗的相应数学模型。标志物的具体例子包括多种免疫细胞,遗传多态性,miRNA,表观遗传学,免疫组化和分子生物学“信标”,例如细胞表面蛋白,细胞因子,信号蛋白和酶。我们确定了与肿瘤相关的巨噬细胞(TAMs),人类白细胞抗原(HLA)I类,Ki-67 / CK20,IL-2,IL-8和IL-6 / IL-10比值的组合是两者最有希望的标志适用于模拟研究的BCG前后治疗。这些数据的复杂性和针对特定患者的性质保证了将强大的多参数数学方法与分子/细胞生物学洞察力和临床投入结合使用。

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