Literature DB >> 30528182

Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) model: A good alternative to study PCa progression and chemoprevention approaches.

Larissa Akemi Kido1, Celina de Almeida Lamas2, Mário Roberto Maróstica3, Valéria Helena Alves Cagnon2.   

Abstract

The use of genetically modified animals has been studied in scientific research over time as a way to discover new treatments or even a cure for various diseases. Transgenic Adenocarcinoma of the Mouse Prostate (TRAMP) is a model for prostate cancer (PCa) that develops lesions that range from preneoplastic to metastasis. Its similarity to human PCa brings essential knowledge about disease development as well as making possible to investigate different degrees of the tumor profile. We reviewed the literature regarding five important areas relating to PCa progression in the TRAMP model. We also present some useful PCa models comparing them to TRAMP. Furthermore, we investigated the effect of some therapies related to these areas highlighting the best approaches that can delay PCa progression. The revised studies showed that TRAMP cancer stages are well established from 8 to 30 weeks of age, which makes possible to interfere in specific times of PCa development. Moreover, inflammatory and angiogenic blockage before the appearance of malignant lesions retarded PCa progression and showed better results than therapeutical approaches in other phases in TRAMP mice. Reactive stroma is less studied than other areas, although it has been showing a particular relevance in PCa as a milestone in malignant transformation through the modulation of TGF-β, vimentin, and αSMA. We concluded that even years after its creation, the TRAMP model is still one of the most essential tools for PCa study, as well as for the development of new strategies to prevent the disease.
Copyright © 2018 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Angiogenesis; Inflammation; Prostate; Reactive stroma; TRAMP

Mesh:

Substances:

Year:  2018        PMID: 30528182     DOI: 10.1016/j.lfs.2018.12.002

Source DB:  PubMed          Journal:  Life Sci        ISSN: 0024-3205            Impact factor:   5.037


  7 in total

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2.  Dimethylaminomicheliolide Sensitizes Cancer Cells to Radiotherapy for Synergistic Combination with Immune Checkpoint Blockade.

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Journal:  Adv Ther (Weinh)       Date:  2021-10-03

3.  Systemic Ablation of Camkk2 Impairs Metastatic Colonization and Improves Insulin Sensitivity in TRAMP Mice: Evidence for Cancer Cell-Extrinsic CAMKK2 Functions in Prostate Cancer.

Authors:  Thomas L Pulliam; Dominik Awad; Jenny J Han; Mollianne M Murray; Jeffrey J Ackroyd; Pavithr Goli; Jonathan S Oakhill; John W Scott; Michael M Ittmann; Daniel E Frigo
Journal:  Cells       Date:  2022-06-10       Impact factor: 7.666

Review 4.  Growth/Differentiation Factor-15 (GDF-15): From Biomarker to Novel Targetable Immune Checkpoint.

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5.  Resistance to Androgen Deprivation Leads to Altered Metabolism in Human and Murine Prostate Cancer Cell and Tumor Models.

Authors:  Jinny Sun; Robert A Bok; Justin DeLos Santos; Deepti Upadhyay; Romelyn DeLos Santos; Shubhangi Agarwal; Mark Van Criekinge; Daniel B Vigneron; Rahul Aggarwal; Donna M Peehl; John Kurhanewicz; Renuka Sriram
Journal:  Metabolites       Date:  2021-02-26

6.  N6-methyladenosine RNA methylation regulators contribute to the progression of prostate cancer.

Authors:  Qunying Wu; Xing Xie; Yiming Huang; Shanshan Meng; Youcheng Li; Huifeng Wang; Yanling Hu
Journal:  J Cancer       Date:  2021-01-01       Impact factor: 4.207

7.  rAAV-delivered PTEN therapeutics for prostate cancer.

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Journal:  Mol Ther Nucleic Acids       Date:  2021-11-29       Impact factor: 10.183

  7 in total

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