Abstract

Intrinsic resistance to anti-HER2 therapy in breast cancer remains an obstacle in the clinic, limiting its efficacy. However, the biological basis for intrinsic resistance is poorly understood. Here we performed a CRISPR/Cas9-mediated loss-of-function genetic profiling and identified TALDO1, which encodes the rate-limiting transaldolase (TA) enzyme in the non-oxidative pentose phosphate pathway, as essential for cellular survival following pharmacological HER2 blockade. Suppression of TA increases cell susceptibility to HER2 inhibition in two intrinsically resistant breast cancer cell lines with HER2 amplification. Mechanistically, TA depletion combined with HER2 inhibition significantly reduces cellular NADPH levels, resulting in excessive ROS production and deficient lipid and nucleotide synthesis. Importantly, higher TA expression correlates with poor response to HER2 inhibition in a breast cancer patient cohort. Together, these results pinpoint TA as a novel metabolic enzyme possessing synthetic lethality with HER2 inhibition that can potentially be exploited as a biomarker or target for combination therapy.

Details

Title
Synthetic lethality between HER2 and transaldolase in intrinsically resistant HER2-positive breast cancers
Author
Ding, Yi 1 ; Chang, Gong 2 ; Huang, De 1 ; Chen, Rui 1 ; Pinpin Sui 3 ; Lin, Kevin H 1 ; Liang, Gehao 2 ; Yuan, Lifeng 1 ; Xiang, Handan 1 ; Chen, Junying 2 ; Yin, Tao 1 ; Alexander, Peter B 1 ; Qian-Fei, Wang 3 ; Er-Wei, Song 2 ; Qi-Jing, Li 4 ; Wood, Kris C 1 ; Xiao-Fan, Wang 1 

 Department of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA 
 Breast Tumor Center, Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University, Guangzhou, China 
 Key Laboratory of Genomic and Precision Medicine, Collaborative Innovation Center of Genetics and Development, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China 
 Department of Immunology, Duke University Medical Center, Durham, NC, USA 
Pages
1-11
Publication year
2018
Publication date
Oct 2018
Publisher
Nature Publishing Group
e-ISSN
20411723
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2120171242
Copyright
© 2018. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.