PROteolysis Targeting Chimeras: A new cutting-edge nanomedicine for colorectal cancer

Swastika Maitra , Nobendu Mukerjee , Dattatreya Mukherjee , Arabinda Ghosh , Athanasios T. Alexiou

Clinical and Translational Discovery ›› 2024, Vol. 4 ›› Issue (4) : e337

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Clinical and Translational Discovery ›› 2024, Vol. 4 ›› Issue (4) :e337 DOI: 10.1002/ctd2.337
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PROteolysis Targeting Chimeras: A new cutting-edge nanomedicine for colorectal cancer
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Abstract

Colorectal cancer (CRC) is a prevalent malignancy with a high mortality rate, necessitating innovative treatment strategies. PROTACs (PROteolysis Targeting Chimeras) represent a promising therapeutic approach by targeting and degrading oncogenic proteins via the ubiquitin-proteasome pathway. This study explores the potential of using exosomes as delivery vehicles for PROTACs to enhance treatment efficacy. Exosomes, due to their biocompatibility and inherent targeting capabilities, offer a precise method for delivering PROTACs to CRC cells, potentially overcoming challenges associated with traditional therapies such as drug resistance and off-target effects. By harnessing the advantages of both exosome-based delivery and PROTAC technology, this approach aims to improve targeted protein degradation and therapeutic outcomes in CRC treatment. Further research is required to optimize exosome engineering, ensure efficient PROTAC loading, and validate the safety and efficacy of this novel therapeutic strategy through preclinical and clinical trials.

Keywords

colorectal cancer (CRC) / exosome-based delivery / nanomedicine / PROTACs (PROteolysis Targeting Chimeras) / targeted protein degradation

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Swastika Maitra, Nobendu Mukerjee, Dattatreya Mukherjee, Arabinda Ghosh, Athanasios T. Alexiou. PROteolysis Targeting Chimeras: A new cutting-edge nanomedicine for colorectal cancer. Clinical and Translational Discovery, 2024, 4 (4) : e337 DOI:10.1002/ctd2.337

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References

[1]

Sung H, Ferlay J, Siegel RL, et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209-249.

[2]

Ou QL, Chang YL, Liu JH, et al. Mapping the intellectual structure and landscape of colorectal cancer immunotherapy: a bibliometric analysis. Hum Vaccin Immunother. 2024;20(1):2323861.

[3]

Lee MS, Chiou SY, Hsu FC, et al. The effectiveness of 23-valent pneumococcal polysaccharide vaccine on elderly colorectal cancer long-term survivors: a population-based exact-matched cohort study. Hum Vaccin Immunother. 2024;20(1):2350093.

[4]

Sun L, Wang F, Wang X, Zhang F, Ma S, Lv J. SATB1 mediated tumour colonization and β-catenin nuclear localization are associated with colorectal cancer progression. Cancer Biol Ther. 2024;25(1):2320307.

[5]

Liu Y, Cheng DH, Su ZY, et al. Effects of total coumarins from Pileostegia tomentella on exosomal miRNA expression and angiogenesis in colorectal cancer cells. Pharm Biol. 2024;62(1):153-161.

[6]

Ma Z, Wei K, Yang F, et al. Tumor-derived exosomal miR-3157-3p promotes angiogenesis, vascular permeability and metastasis by targeting TIMP/KLF2 in non-small cell lung cancer. Cell Death Dis. 2021;12(9):840.

[7]

Liu L, Zhao M, Lang X, et al. Modified Lichong decoction intervenes in colorectal cancer by modulating the intestinal flora and the Wnt/β-catenin signaling pathway. J Cancer Res Clin Oncol. 2024;150(5):234.

[8]

Fong W, Li Q, Yu J. Gut microbiota modulation: a novel strategy for prevention and treatment of colorectal cancer. Oncogene. 2020;39(26):4925-4943.

[9]

Zhang D, Ma B, Dragovich PS, et al. Tissue distribution and retention drives efficacy of rapidly clearing VHL-based PROTACs. Commun Med. 2024;4(1):87.

[10]

Mohite P, Yadav V, Pandhare R, et al. Revolutionizing cancer treatment: unleashing the power of viral vaccines, monoclonal antibodies, and PROteolysis-TArgeting Chimeras in the new era of immunotherapy. ACS Omega. 2024;9(7):7277-7295.

[11]

Liang G, Zhu Y, Ali DJ, et al. Engineered exosomes for targeted co-delivery of miR-21 inhibitor and chemotherapeutics to reverse drug resistance in colon cancer. J Nanobiotechnology. 2020;18(1):10.

[12]

Mukerjee N, Maitra S, Ghosh A, Alexiou A, Thorat ND. Exosome-mediated PROTAC delivery for treatment of RNA viral infections and zoonoses. Drug Discov Today. 2024:104044.

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2024 The Author(s). Clinical and Translational Discovery published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics.

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