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α-klotho与人类恶性肿瘤的治疗

Klotho and the Treatment of Human Malignancies.

作者信息

Sachdeva Aishani, Gouge Jerome, Kontovounisios Christos, Nikolaou Stella, Ashworth Alan, Lim Kenneth, Chong Irene

机构信息

The Royal Marsden NHS Foundation Trust, London SW6 6JJ, UK.

Department of Surgery and Cancer, Chelsea and Westminster Hospital, London SW10 9NH, UK.

出版信息

Cancers (Basel). 2020 Jun 23;12(6):1665. doi: 10.3390/cancers12061665.

Abstract

Klotho was first discovered as an anti-ageing protein linked to a number of age-related disease processes, including cardiovascular, renal, musculoskeletal, and neurodegenerative conditions. Emerging research has also demonstrated a potential therapeutic role for Klotho in cancer biology, which is perhaps unsurprising given that cancer and ageing share similar molecular hallmarks. In addition to functioning as a tumour suppressor in numerous solid tumours and haematological malignancies, Klotho represents a candidate therapeutic target for patients with these diseases, the majority of whom have limited treatment options. Here, we examine contemporary evidence evaluating the anti-neoplastic effects of Klotho and describe the modulation of downstream oncogenic signalling pathways, including Wnt/β-catenin, FGF, IGF1, PIK3K/AKT, TGFβ, and the Unfolded Protein Response. We also discuss possible approaches to developing therapeutic Klotho and consider technological advances that may facilitate the delivery of Klotho through gene therapy.

摘要

klotho最初被发现是一种与多种年龄相关疾病过程相关的抗衰老蛋白,这些疾病过程包括心血管、肾脏、肌肉骨骼和神经退行性疾病。新兴研究还证明了klotho在癌症生物学中的潜在治疗作用,考虑到癌症和衰老具有相似的分子特征,这也许并不奇怪。除了在许多实体瘤和血液系统恶性肿瘤中作为肿瘤抑制因子发挥作用外,klotho还代表了这些疾病患者的候选治疗靶点,其中大多数患者的治疗选择有限。在这里,我们研究了评估klotho抗肿瘤作用的当代证据,并描述了下游致癌信号通路的调节,包括Wnt/β-连环蛋白、FGF、IGF1、PIK3K/AKT、TGFβ和未折叠蛋白反应。我们还讨论了开发治疗性klotho的可能方法,并考虑了可能有助于通过基因疗法递送klotho的技术进步。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7faf/7352559/2f8ca0162b58/cancers-12-01665-g001.jpg

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