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Reduced Taurine Synthesis Underlies Morphine-Promoted Lung Metastasis of Triple-Negative Breast Cancer
Shih-Hong Chen1,2, Ting-Ling Ke1, Chien-Hung Shih1
1Institute of Molecular Medicine, National Tsing Hua University, Hsinchu 300044, Taiwan.
Abstract:
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.
Insights
Extended morphine exposure increases triple-negative breast cancer (TNBC) metastasis by downregulating taurine biosynthesis. Taurine may mitigate morphine-induced invasion, offering a potential supplement for TNBC patients undergoing morphine treatment.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Triple-negative breast cancer (TNBC) progression and metastasis mechanisms under extended morphine exposure are poorly understood.
- Extended morphine use is a concern, particularly for cancer patients with poor prognoses.
- Investigating morphine's impact on TNBC is crucial for patient outcomes.
Purpose of the Study:
- To investigate the impact of extended morphine treatment on TNBC transcriptional profiles.
- To identify molecular mechanisms linking morphine exposure to TNBC metastasis.
- To explore potential therapeutic interventions for morphine-associated TNBC progression.
Main Methods:
- Mice received intraperitoneal morphine for 14 days before EO771 TNBC cell implantation.
- Tumor growth, metastasis, and RNA expression were analyzed after primary tumor removal and continued morphine/saline administration.
- RNA sequencing and pathway analysis identified changes in taurine/hypotaurine biosynthesis.
Main Results:
- Extended morphine exposure significantly increased lung metastasis in a TNBC mouse model.
- Morphine treatment downregulated taurine/hypotaurine biosynthesis and decreased GAD1 expression.
- Taurine mitigated morphine-induced EO771 cell invasion, but not that induced by droperidol or naloxone.
Conclusions:
- Morphine-induced reduction in GAD1 expression and taurine biosynthesis may drive TNBC metastasis.
- Taurine shows potential to counteract morphine-induced cancer cell invasion.
- Taurine may serve as a beneficial supplement for TNBC patients requiring morphine therapy.
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