Reduced Taurine Synthesis Underlies Morphine-Promoted Lung Metastasis of Triple-Negative Breast Cancer

被引:0
作者
Chen, Shih-Hong [1 ,2 ]
Ke, Ting-Ling [1 ]
Shih, Chien-Hung [1 ]
Hsiung, Chia-Ni [1 ]
Chen, Kuo-Chin [1 ]
Huang, Zi-Xuan [1 ]
Chuang, Tsung-Hsien [3 ]
Chen, Li-Kuei [4 ,5 ]
Chen, Linyi [1 ,6 ]
机构
[1] Natl Tsing Hua Univ, Inst Mol Med, Hsinchu 30013, Taiwan
[2] Cathay Gen Hosp Med Ctr, Dept Anesthesiol, Taipei, Taiwan
[3] Natl Hlth Res Inst, Immunol Res Ctr, Miaoli 350401, Taiwan
[4] China Med Univ, Coll Med, Taichung 406040, Taiwan
[5] China Med Univ Hosp, Dept Anesthesiol, Taichung 404327, Taiwan
[6] Natl Tsing Hua Univ, Dept Med Sci, Hsinchu 300044, Taiwan
关键词
cysteine dioxygenase type; glutamate decarboxylase 1; morphine usage; taurine biosynthesis; triple-negative breast cancer; MU-OPIOID RECEPTOR; GENE ONTOLOGY; ANGIOGENESIS; PROLIFERATION; APOPTOSIS; PROTEINS; PACKAGE; CELLS; MODEL; ROLES;
D O I
10.3390/cancers17071086
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The mechanisms underlying the progression and metastasis of triple-negative breast cancer (TNBC) in the context of extended morphine exposure remain poorly understood. Morphine consumption has been a pressing issue in many countries. While the physiological impact of extended morphine use is multifaceted, cancer patients with a history of extended morphine usage often have a poor prognosis. Methods: In this study, we investigated the impact of extended morphine treatment on the transcriptional profiles of TNBC. To this end, mice were administered morphine intraperitoneally for 14 days, followed by the implantation of EO771 cells, which are triple-negative breast cancer cells, into their mammary fat pad. After primary tumors were removed on the 38th day, a subset of mice was continuously given saline or morphine until the 68th day. Tumor size, organ metastasis, and tumor RNA expression were analyzed. Results: Our findings showed that extended exposure to morphine led to an increase in lung metastasis in the mouse model of triple-negative breast cancer. We analyzed RNA sequencing on tumors to compare their transcriptional profiles with or without metastasis. Through pathway analysis, we specifically examined the novel impact of morphine on the downregulation of taurine/hypotaurine biosynthesis. Given that morphine, droperidol (a dopamine receptor antagonist), and naloxone (an opioid receptor antagonist) might act through either opioid receptors or dopamine receptors, we further demonstrated that taurine mitigated EO771 cell invasion induced by morphine but not by droperidol or naloxone treatment. Additionally, morphine treatment markedly decreased the expression of GAD1, one of the enzymes essential for taurine biosynthesis, whereas droperidol and naloxone did not. Conclusions: The findings of morphine-induced reduction in GAD1 levels and the inhibition of invasion by taurine treatment suggest that taurine could serve as a potential supplement for triple-negative breast cancer patients who require morphine as part of their treatment regimen or due to their circumstances.
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页数:22
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