Department of Chemistry, Brandeis University, 415 South Street, Waltham, MA, 02453, USA.
Bioinspired Soft Matter Unit, Okinawa Institute of Science and Technology Graduate University, 1919-1 Tancha, Onna-son, Okinawa, 904-0495, Japan.
Chemistry. 2020 Nov 26;26(66):15116-15120. doi: 10.1002/chem.202002974. Epub 2020 Oct 15.
Although lipids contribute to cancer drug resistance, it is challenging to target diverse range of lipids. Here, we show enzymatically inserting exceedingly simple synthetic lipids into membranes for increasing membrane tension and selectively inhibiting drug resistant cancer cells. The lipid, formed by conjugating dodecylamine to d-phosphotyrosine, self-assembles to form micelles. Enzymatic dephosphorylation of the micelles inserts the lipids into membranes and increases membrane tension. The micelles effectively inhibit a drug resistant glioblastoma cell (T98G) or a triple-negative breast cancer cell (HCC1937), without inducing acquired drug resistance. Moreover, the enzymatic reaction of the micelles promotes the accumulation of the lipids in the membranes of subcellular organelles (e.g., endoplasmic reticulum (ER), Golgi, and mitochondria), thus activating multiple regulated cell death pathways. This work, in which for the first time membrane tension is increased to inhibit cancer cells, illustrates a new and powerful supramolecular approach for antagonizing difficult drug targets.
尽管脂质有助于癌症药物耐药性,但靶向多种脂质具有挑战性。在这里,我们展示了通过酶促将极其简单的合成脂质插入到膜中,以增加膜张力并选择性地抑制耐药性癌细胞。该脂质由将十二胺与 D-磷酸酪氨酸偶联形成,可自组装成胶束。胶束的酶促去磷酸化将脂质插入到膜中并增加膜张力。这些胶束有效地抑制了耐药性神经胶质瘤细胞(T98G)或三阴性乳腺癌细胞(HCC1937),而不会诱导获得性耐药性。此外,胶束的酶促反应促进了脂质在亚细胞细胞器(如内质网(ER)、高尔基体和线粒体)的膜中的积累,从而激活了多种受调控的细胞死亡途径。这项工作首次通过增加膜张力来抑制癌细胞,说明了一种针对难以靶向药物的新型和强大的超分子方法。