Muellner Markus K, Mair Barbara, Ibrahim Yasir, Kerzendorfer Claudia, Lechtermann Hannelore, Trefzer Claudia, Klepsch Freya, Müller André C, Leitner Ernestine, Macho-Maschler Sabine, Superti-Furga Giulio, Bennett Keiryn L, Baselga José, Rix Uwe, Kubicek Stefan, Colinge Jacques, Serra Violeta, Nijman Sebastian M B
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, Vienna, Austria.
Experimental Therapeutics Group, Vall d'Hebron Institute of Oncology, Barcelona, Spain.
Mol Syst Biol. 2015 Feb 19;11(1):789. doi: 10.15252/msb.20145664.
Some mutations in cancer cells can be exploited for therapeutic intervention. However, for many cancer subtypes, including triple-negative breast cancer (TNBC), no frequently recurring aberrations could be identified to make such an approach clinically feasible. Characterized by a highly heterogeneous mutational landscape with few common features, many TNBCs cluster together based on their 'basal-like' transcriptional profiles. We therefore hypothesized that targeting TNBC cells on a systems level by exploiting the transcriptional cell state might be a viable strategy to find novel therapies for this highly aggressive disease. We performed a large-scale chemical genetic screen and identified a group of compounds related to the drug PKC412 (midostaurin). PKC412 induced apoptosis in a subset of TNBC cells enriched for the basal-like subtype and inhibited tumor growth in vivo. We employed a multi-omics approach and computational modeling to address the mechanism of action and identified spleen tyrosine kinase (SYK) as a novel and unexpected target in TNBC. Quantitative phosphoproteomics revealed that SYK inhibition abrogates signaling to STAT3, explaining the selectivity for basal-like breast cancer cells. This non-oncogene addiction suggests that chemical SYK inhibition may be beneficial for a specific subset of TNBC patients and demonstrates that targeting cell states could be a viable strategy to discover novel treatment strategies.
癌细胞中的一些突变可用于治疗干预。然而,对于许多癌症亚型,包括三阴性乳腺癌(TNBC),尚未发现频繁复发的畸变,以使这种方法在临床上可行。许多TNBC具有高度异质性的突变图谱,几乎没有共同特征,它们基于“基底样”转录谱聚集在一起。因此,我们假设通过利用转录细胞状态在系统水平上靶向TNBC细胞可能是为这种高度侵袭性疾病寻找新疗法的可行策略。我们进行了大规模化学遗传筛选,鉴定出一组与药物PKC412(米哚妥林)相关的化合物。PKC412在富含基底样亚型的TNBC细胞亚群中诱导凋亡,并在体内抑制肿瘤生长。我们采用多组学方法和计算模型来研究其作用机制,并确定脾酪氨酸激酶(SYK)是TNBC中一个新的意外靶点。定量磷酸化蛋白质组学表明,SYK抑制可消除向STAT3的信号传导,解释了对基底样乳腺癌细胞的选择性。这种非癌基因成瘾表明,化学抑制SYK可能对特定亚群的TNBC患者有益,并证明靶向细胞状态可能是发现新治疗策略的可行策略。