Literature DB >> 29476017

Administration of Hypoxia-Activated Prodrug Evofosfamide after Conventional Adjuvant Therapy Enhances Therapeutic Outcome and Targets Cancer-Initiating Cells in Preclinical Models of Colorectal Cancer.

Jennifer Haynes1, Trevor D McKee1,2, Andrew Haller1, Yadong Wang1, Cherry Leung1, Deena M A Gendoo1,3, Evelyne Lima-Fernandes4, Antonija Kreso1, Robin Wolman1, Eva Szentgyorgyi5, Douglass C Vines1,2,6, Benjamin Haibe-Kains1,3,7, Bradly G Wouters1,3,6, Ur Metser1,8,9, David A Jaffray1,2,3,6,9, Myles Smith10, Catherine A O'Brien11,12,13,14.   

Abstract

Purpose: Cancer-initiating cells (C-IC) have been described in multiple cancer types, including colorectal cancer. C-ICs are defined by their capacity to self-renew, thereby driving tumor growth. C-ICs were initially thought to be static entities; however, recent studies have determined these cells to be dynamic and influenced by microenvironmental cues such as hypoxia. If hypoxia drives the formation of C-ICs, then therapeutic targeting of hypoxia could represent a novel means to target C-ICs.Experimental Design: Patient-derived colorectal cancer xenografts were treated with evofosfamide, a hypoxia-activated prodrug (HAP), in combination with 5-fluorouracil (5-FU) or chemoradiotherapy (5-FU and radiation; CRT). Treatment groups included both concurrent and sequential dosing regimens. Effects on the colorectal cancer-initiating cell (CC-IC) fraction were assessed by serial passage in vivo limiting dilution assays. FAZA-PET imaging was utilized as a noninvasive method to assess intratumoral hypoxia.
Results: Hypoxia was sufficient to drive the formation of CC-ICs and colorectal cancer cells surviving conventional therapy were more hypoxic and C-IC-like. Using a novel approach to combination therapy, we show that sequential treatment with 5-FU or CRT followed by evofosfamide not only inhibits tumor growth of xenografts compared with 5-FU or CRT alone, but also significantly decreases the CC-IC fraction. Furthermore, noninvasive FAZA-PET hypoxia imaging was predictive of a tumor's response to evofosfamide.Conclusions: Our data demonstrate a novel means to target the CC-IC fraction by adding a HAP sequentially after conventional adjuvant therapy, as well as the use of FAZA-PET as a biomarker for hypoxia to identify tumors that will benefit most from this approach. Clin Cancer Res; 24(9); 2116-27. ©2018 AACR. ©2018 American Association for Cancer Research.

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Year:  2018        PMID: 29476017     DOI: 10.1158/1078-0432.CCR-17-1715

Source DB:  PubMed          Journal:  Clin Cancer Res        ISSN: 1078-0432            Impact factor:   12.531


  11 in total

Review 1.  Hypoxia in solid tumors: a key promoter of cancer stem cell (CSC) resistance.

Authors:  Masoud Najafi; Bagher Farhood; Keywan Mortezaee; Ebrahim Kharazinejad; Jamal Majidpoor; Reza Ahadi
Journal:  J Cancer Res Clin Oncol       Date:  2019-11-16       Impact factor: 4.553

Review 2.  Lipid metabolic reprogramming by hypoxia-inducible factor-1 in the hypoxic tumour microenvironment.

Authors:  Jieun Seo; Jeong-Eun Yun; Sung Joon Kim; Yang-Sook Chun
Journal:  Pflugers Arch       Date:  2022-03-28       Impact factor: 3.657

Review 3.  Hypoxia effects on cancer stem cell phenotype in colorectal cancer: a mini-review.

Authors:  Mateus de Almeida Rainho; Andre Luiz Mencalha; Alessandra Alves Thole
Journal:  Mol Biol Rep       Date:  2021-10-12       Impact factor: 2.316

Review 4.  Functionalized Nitroimidazole Scaffold Construction and Their Pharmaceutical Applications: A 1950-2021 Comprehensive Overview.

Authors:  Ria Gupta; Sumit Sharma; Rohit Singh; Ram A Vishwakarma; Serge Mignani; Parvinder Pal Singh
Journal:  Pharmaceuticals (Basel)       Date:  2022-04-30

Review 5.  How to Modulate Tumor Hypoxia for Preclinical In Vivo Imaging Research.

Authors:  Sven De Bruycker; Christel Vangestel; Steven Staelens; Tim Van den Wyngaert; Sigrid Stroobants
Journal:  Contrast Media Mol Imaging       Date:  2018-10-18       Impact factor: 3.161

6.  Deep-learning and MR images to target hypoxic habitats with evofosfamide in preclinical models of sarcoma.

Authors:  Bruna V Jardim-Perassi; Wei Mu; Suning Huang; Michal R Tomaszewski; Jan Poleszczuk; Mahmoud A Abdalah; Mikalai M Budzevich; William Dominguez-Viqueira; Damon R Reed; Marilyn M Bui; Joseph O Johnson; Gary V Martinez; Robert J Gillies
Journal:  Theranostics       Date:  2021-03-11       Impact factor: 11.556

Review 7.  The Hypoxia-Activated Prodrug TH-302: Exploiting Hypoxia in Cancer Therapy.

Authors:  Yue Li; Long Zhao; Xiao-Feng Li
Journal:  Front Pharmacol       Date:  2021-04-19       Impact factor: 5.810

8.  CRISPR screens identify cholesterol biosynthesis as a therapeutic target on stemness and drug resistance of colon cancer.

Authors:  Shanshan Gao; Fraser Soares; Shiyan Wang; Chi Chun Wong; Huarong Chen; Zhenjie Yang; Weixin Liu; Minnie Y Y Go; Musaddeque Ahmed; Yong Zeng; Catherine Adell O'Brien; Joseph J Y Sung; Housheng Hansen He; Jun Yu
Journal:  Oncogene       Date:  2021-10-07       Impact factor: 9.867

9.  Phase Ib dose-escalation study of the hypoxia-modifier Myo-inositol trispyrophosphate in patients with hepatopancreatobiliary tumors.

Authors:  Marcel A Schneider; Michael Linecker; Ralph Fritsch; Urs J Muehlematter; Daniel Stocker; Bernhard Pestalozzi; Panagiotis Samaras; Alexander Jetter; Philipp Kron; Henrik Petrowsky; Claude Nicolau; Jean-Marie Lehn; Bostjan Humar; Rolf Graf; Pierre-Alain Clavien; Perparim Limani
Journal:  Nat Commun       Date:  2021-06-21       Impact factor: 14.919

10.  Quantitative Visualization of Hypoxia and Proliferation Gradients Within Histological Tissue Sections.

Authors:  Mark Zaidi; Fred Fu; Dan Cojocari; Trevor D McKee; Bradly G Wouters
Journal:  Front Bioeng Biotechnol       Date:  2019-12-05
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