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肿瘤和宿主微生物群在泌尿生殖系统癌症免疫治疗反应中的作用

The Role of Tumor and Host Microbiome on Immunotherapy Response in Urologic Cancers.

作者信息

Pfail John, Drobner Jake, Doppalapudi Krishna, Saraiya Biren, Packiam Vignesh, Ghodoussipour Saum

机构信息

Section of Urologic Oncology, Rutgers Cancer Institute of New Jersey and Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA.

Department of Medicine, Division of Medical Oncology, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ, USA.

出版信息

J Cancer Immunol (Wilmington). 2024;6(1):1-13. doi: 10.33696/cancerimmunol.6.078.

Abstract

INTRODUCTION & OBJECTIVE: The role of the microbiome in the development and treatment of genitourinary malignancies is just starting to be appreciated. Accumulating evidence suggests that the microbiome can modulate immunotherapy through signaling in the highly dynamic tumor microenvironment. Nevertheless, much is still unknown about the immuno-oncology-microbiome axis, especially in urologic oncology. The objective of this review is to synthesize our current understanding of the microbiome's role in modulating and predicting immunotherapy response to genitourinary malignancies.

METHODS

A literature search for peer-reviewed publications about the microbiome and immunotherapy response in bladder, kidney, and prostate cancer was conducted. All research available in PubMed, Google Scholar, clinicaltrials.gov, and bioRxiv up to September 2023 was analyzed.

RESULTS

Significant differences in urinary microbiota composition have been found in patients with genitourinary cancers compared to healthy controls. Lactic acid-producing bacteria, such as and genera, may have value in augmenting BCG responsiveness to bladder cancer. BCG may also be a dynamic regulator of PD-L1. Thus, the combination of BCG and immune checkpoint inhibitors may be an effective strategy for bladder cancer management. In advanced renal cell carcinoma, studies show that recent antibiotic administration negatively impacts survival outcomes in patients undergoing immunotherapy, while administration of CBM588, a live bacterial product, is associated with improved progression-free survival. Specific bacterial taxa, such as , have been linked with response to pembrolizumab in metastatic castrate-resistant prostate cancer. Fecal microbiota transplant has been shown to overcome resistance and reduce toxicity to immunotherapy; it is currently being investigated for both kidney and prostate cancers.

CONCLUSIONS

Although the exact mechanism is unclear, several studies identify a symbiotic relationship between microbiota-centered interventions and immunotherapy efficacy. It is possible to improve immunotherapy responsiveness in genitourinary malignancies using the microbiome, but further research with more standardized methodology is warranted.

摘要

引言与目的

微生物群在泌尿生殖系统恶性肿瘤的发生发展及治疗中的作用才刚刚开始受到重视。越来越多的证据表明,微生物群可通过在高度动态的肿瘤微环境中发出信号来调节免疫治疗。然而,关于免疫肿瘤学与微生物群轴,尤其是在泌尿肿瘤学方面,仍有许多未知之处。本综述的目的是综合我们目前对微生物群在调节和预测泌尿生殖系统恶性肿瘤免疫治疗反应中作用的理解。

方法

对关于微生物群与膀胱癌、肾癌和前列腺癌免疫治疗反应的同行评审出版物进行文献检索。分析了截至2023年9月在PubMed、谷歌学术、clinicaltrials.gov和bioRxiv上可获得的所有研究。

结果

与健康对照相比,在泌尿生殖系统癌症患者中发现了尿微生物群组成的显著差异。产乳酸细菌,如某属和某属,可能在增强卡介苗对膀胱癌的反应性方面具有价值。卡介苗也可能是程序性死亡受体1配体(PD-L1)的动态调节剂。因此,卡介苗与免疫检查点抑制剂联合使用可能是膀胱癌治疗的有效策略。在晚期肾细胞癌中,研究表明近期使用抗生素会对接受免疫治疗的患者的生存结果产生负面影响,而给予活菌产品CBM588与无进展生存期的改善相关。特定的细菌分类群,如某菌属,已被证明与转移性去势抵抗性前列腺癌患者对帕博利珠单抗的反应有关。粪便微生物群移植已被证明可克服耐药性并降低免疫治疗的毒性;目前正在对肾癌和前列腺癌进行研究。

结论

尽管确切机制尚不清楚,但多项研究确定了以微生物群为中心的干预措施与免疫治疗疗效之间的共生关系。利用微生物群有可能提高泌尿生殖系统恶性肿瘤的免疫治疗反应性,但需要采用更标准化的方法进行进一步研究。

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本文引用的文献

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The Association Between the Urinary Microbiome and Bladder Cancer.尿微生物组与膀胱癌的关系。
Urol Clin North Am. 2023 Feb;50(1):81-89. doi: 10.1016/j.ucl.2022.09.012.
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Bacteria for Treatment: Microbiome in Bladder Cancer.用于治疗的细菌:膀胱癌中的微生物群
Biomedicines. 2022 Jul 25;10(8):1783. doi: 10.3390/biomedicines10081783.
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Bladder cancer, inflammageing and microbiomes.膀胱癌、炎症与微生物组。
Nat Rev Urol. 2022 Aug;19(8):495-509. doi: 10.1038/s41585-022-00611-3. Epub 2022 Jul 7.
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Microbiota in health and diseases.肠道菌群与健康和疾病。
Signal Transduct Target Ther. 2022 Apr 23;7(1):135. doi: 10.1038/s41392-022-00974-4.

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