Large scale in vivo micro‐RNA loss of function screen identified miR‐29a, miR‐100 and miR‐155 as modulators of radioresistance and tumor‐stroma communication

• Published in: International journal of cancer 2019-06, Vol.144 (11), p.2774-2781
• Main Authors: Fahim Golestaneh, Azadeh, Lecker, Laura S.M., Schlegel, Julian, Nowrouzi, Ali, Schwager, Christian, Meister, Sarah, Weichert, Wilko, Debus, Jürgen, Abdollahi, Amir
• Format: Article
• Language: English
• Subjects: Angiogenesis; Apoptosis; Brain tumors; Cancer; Caspase; Caspase-3; DNA damage; DNA damage response; Double-strand break repair; functional genomics; Gene expression; Ionizing radiation; Irradiation; Latency; Medical research; micro RNA; Phenotypes; Radiation therapy; Radioresistance; Radiosensitivity; Regulators; Ribonucleic acid; RNA; Stroma; Survival; Tumor cells; Tumors; Vascular endothelial growth factor
• ISSN: 0020-7136; 1097-0215
• DOI: 10.1002/ijc.32019

Micro RNAs (miR) are master regulators of cellular transcriptome. We aimed to investigate the role of miR regulation on tumor radiosensitivity and development of local tumor recurrence by a novel large‐scale in vivo loss of function screen. For stable miR silencing, human A431 tumor cells were transduced with lentiviral constructs against 170 validated human miR (miRzip library). Fractionated radiotherapy (5x6Gy) was applied to A431 miRzip library growing s.c. in NCr nude mice. Enrichment of miRZip and miR expression was assessed using multiplexed qRT‐PCR. The modulatory effect of miR on tumor and tumor microenvironment response to ionizing radiation was further evaluated by clonogenic survival, apoptosis (Caspase 3/7), DNA double‐strand breaks (DSB, nuclear γH2AX foci), tumor microvessel density (MVD), transcriptome and protein analysis. Fractionated irradiation of the A431 miRzip library led to regression of tumors. However, after a latency period, tumors ultimately progressed and formed local recurrences indicating the survival of a subpopulation of miRzip expressing tumor clones. Among the selected miR for subsequent validation studies, loss of miR‐29a, miR‐100 and miR‐155 was found to enhance clonogenic survival, reduce apoptosis and residual γH2AX foci of irradiated tumor cells. Moreover, knockdown of miR increased tumor angiogenesis correlating with elevated VEGF and TGFα expression levels. This phenomenon was most evident after tumor irradiation in vivo suggesting a critical role for tumor‐stroma communication in development of the radioresistant phenotype. Engineering radioresistant tumors in vivo by modulating miR expression may lead to identification of critical targets for conquering local therapy failure. What's new? Acquired tumor radioresistance is a major obstacle in cancer treatment. Although microRNAs have emerged as master regulators of the cellular transcriptome, their roles in the molecular mechanisms underlying therapy resistance and local tumor recurrence remain elusive. Here, the authors report the first large‐scale in‐vivo loss of miR function screen for discovery of novel miR regulators of tumor radioresistance after fractionated irradiation. Loss of miR‐29a, miR‐100, and miR‐155 was found to elicit a radioprotective effect correlating with reduced apoptosis and residual radiation‐induced foci. Furthermore, the data shed light on the importance of in‐vivo selection pressures for evolution of tumor radioresistance.