1] UMR INSERM U1065/UNS, Centre Méditerranéen de Médecine Moléculaire (C3M), Equipe Inflammation, Cancer, Cellules Souches Cancéreuses, Nice, France [2] Université de Nice-Sophia Antipolis, UFR Médecine, Faculté de Médecine, Nice, France.
1] UMR INSERM U1065/UNS, Centre Méditerranéen de Médecine Moléculaire (C3M), Equipe Inflammation, Cancer, Cellules Souches Cancéreuses, Nice, France [2] Université de Nice-Sophia Antipolis, UFR Médecine, Faculté de Médecine, Nice, France [3] Centre Hospitalier Universitaire de Nice, Service d'Oncologie Pédiatrique, Hôpital de l'Archet, Nice, France.
Leukemia. 2015 Jun;29(6):1253-66. doi: 10.1038/leu.2014.338. Epub 2014 Dec 8.
The altered metabolism of cancer cells is a treasure trove to discover new antitumoral strategies. The gene (SLC7A5) encoding system L amino-acid transporter 1 (LAT1) is overexpressed in murine lymphoma cells generated via T-cell deletion of the pten tumor suppressor, and also in human T-cell acute lymphoblastic leukemia (T-ALL)/lymphoma (T-LL) cells. We show here that a potent and LAT1 selective inhibitor (JPH203) decreased leukemic cell viability and proliferation, and induced transient autophagy followed by apoptosis. JPH203 could also alter the in vivo growth of luciferase-expressing-tPTEN-/- cells xenografted into nude mice. In contrast, JPH203 was nontoxic to normal murine thymocytes and human peripheral blood lymphocytes. JPH203 interfered with constitutive activation of mTORC1 and Akt, decreased expression of c-myc and triggered an unfolded protein response mediated by the C/EBP homologous protein (CHOP) transcription factor associated with cell death. A JPH203-resistant tPTEN-/-clone appeared CHOP induction deficient. We also demonstrate that targeting LAT1 may be an efficient broad spectrum adjuvant approach to treat deadly T-cell malignancies as the molecule synergized with rapamycin, dexamethasone, doxorubicin, velcade and l-asparaginase to alter leukemic cell viability.
癌细胞代谢的改变是发现新的抗肿瘤策略的宝库。编码系统 L 氨基酸转运体 1(LAT1)的基因(SLC7A5)在通过 T 细胞缺失肿瘤抑制因子 pten 产生的鼠淋巴瘤细胞中过表达,也在人 T 细胞急性淋巴细胞白血病(T-ALL)/淋巴瘤(T-LL)细胞中过表达。我们在这里表明,一种有效的、选择性的 LAT1 抑制剂(JPH203)降低了白血病细胞的活力和增殖,并诱导短暂的自噬,随后是细胞凋亡。JPH203 还可以改变表达荧光素酶的-tPTEN-/-细胞在裸鼠中的体内生长。相比之下,JPH203 对正常的鼠胸腺细胞和人外周血淋巴细胞没有毒性。JPH203 干扰 mTORC1 和 Akt 的组成性激活,降低 c-myc 的表达,并触发与细胞死亡相关的 C/EBP 同源蛋白(CHOP)转录因子介导的未折叠蛋白反应。一个 JPH203 抗性的 tPTEN-/-克隆出现 CHOP 诱导缺陷。我们还证明,靶向 LAT1 可能是一种有效的广谱辅助治疗致命性 T 细胞恶性肿瘤的方法,因为该分子与雷帕霉素、地塞米松、阿霉素、硼替佐米和 L-天冬酰胺酶协同作用,改变白血病细胞的活力。
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