Qianghu Wang on Muck Rack

Qianghu Wang

As seen in: Nature, Frontiers, Science Magazine, Cell Press
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Articles

Acquired genetic and cell-state changes in IDH-mutant glioma progression

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By Kevin Johnson, Avishay Spitzer, Frederick S. Varn, Masashi Nomura, Luciano Garofano, Tamrin Chowdhury, Anuja Lipsa, Linbin Zhang, Ester Calvo Fernández, Tanyeri Barak, Samirkumar B. Amin, Emre Kocakavuk, Dacheng Zhao, Fulvio D’Angelo, Simona Migliozzi, Lillian Bussema, Simon Gritsch, Sun Ha Paek, Franck Bielle, Alice Laurenge, Bertrand Mathon, Alberto Picca, Marc Sanson, Ann-Christin Hau, Frank Hertel, Kamil Grzyb, Zheng Zhao, Qianghu Wang, Tao Jiang, Julie Miller, Hiroaki Wakimoto, Daniel Cahill, Jennifer Moliterno, Murat Gunel, Beth Hermes, Nader Sanai, Anna Golebiewska, Simone P Niclou, Jason T. Huse, W. K. Alfred Yung, Anna Lasorella, Mario L. Suvà, Antonio Iavarone, Itay Tirosh, Roel G. W. Verhaak, A. Gulhan Ercan-Sencicek, Ayse Buket Peksen, C. Mircea S. Tesileanu, Hyo-Eun Moon
| Nature Verified
Abstract Gliomas with mutant isocitrate dehydrogenase (IDH) are malignant brain tumours that typically arise in early to mid-adulthood and nearly always recur following treatment1,2. However, the genetic and cellular-state changes that drive IDH-mutant glioma progression under treatment remain incompletely understood.
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Stress granules restrain ferroptosis by sequestering ferritin

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By Zehe Ge, Zihan Wang, Mengdie Li, Yunfei Ma, Fangshu Ding, Liuguijie He, Shuhong Sun, Minfeng Tong, Wenxia Xu, Xiefeng Wang, Junxia Zhang, Lingxiang Wu, Yudan Zhang, Lili Niu, Qianghu Wang, Rong Yin, Xiao Li, Yongping You, Jeremy Rich, Xiuxing Wang, Bing Yao, Zhumei Shi, Zhou Yang, Xin Ge, Fang Liu, Bo Chu, Xu Qian, Erjie Zhao, Yizhuo Guo, Longxiu Zhang, Fuwei Tian
| Nature Verified
Abstract Glioblastoma stem cells (GSCs) are refractory to first-line treatment in the clinic, which includes irradiation (IR) and temozolomide (TMZ). Here we find that disrupting stress granules (SGs) sensitizes GSCs to IR/TMZ through ferroptosis. The profiling of SG proteins reveals the recruitment of iron-related proteins including ferritin.
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Inhibiting macrophage-derived lactate transport restores cGAS–STING signalling and enhances antitumour immunity in glioblastoma - Nature Cell Biology

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By Daqi Li, Zhe Zhu, Ryan C Gimple, Yun Chen, Qianghu Wang, Chaojun Li, Nu Zhang, Junxia Zhang, Xu Qian, Qian Zhang, Jeremy Rich
| Nature Verified
Abstract Glioblastoma (GBM) is a malignancy with a complex tumour microenvironment (TME) dominated by GBM stem cells (GSCs) and infiltrated by tumour-associated macrophages (TAMs) and exhibits aberrant metabolic pathways. Lactate is a critical glycolytic metabolite that promotes tumour progression; however, the mechanisms of lactate transport and lactylation in the TME of GBM remain elusive. Here we show that lactate is transported from TAMs to GSCs via MCT4–MCT1.
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