Lidocaine combined with general anesthetics impedes metastasis of breast cancer cells via inhibition of TGF-β/Smad-mediated EMT signaling by reprogramming tumor-associated macrophages

•Anesthetics have a potential impact on the long-term tumor growth, metastasis risk, and recurrence of cancer patients after surgery.•Lidocaine combined with general anesthetics inhibits the metastasis and recurrence of breast cancer by blocking EMT signaling.•Lidocaine not only reduced M2-tumor-ass...

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Veröffentlicht in:International immunopharmacology 2024-12, Vol.142 (Pt B), p.113207, Article 113207
Hauptverfasser: Seok Han, Beom, Ko, Soyeon, Seok Park, Min, Ji Lee, Yun, Eun Kim, Sang, Lee, Pureunchowon, Jin Cho, Ye, Gyeol Go, Han, Kwak, Sehan, Park, Eunji, Lim, Ayoung, Lee, Suji, Yoo, Seungjong, Kim, Hyunzu, Hee Jung, Kyung, Hong, Soon-Sun
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container_end_page
container_issue Pt B
container_start_page 113207
container_title International immunopharmacology
container_volume 142
creator Seok Han, Beom
Ko, Soyeon
Seok Park, Min
Ji Lee, Yun
Eun Kim, Sang
Lee, Pureunchowon
Jin Cho, Ye
Gyeol Go, Han
Kwak, Sehan
Park, Eunji
Lim, Ayoung
Lee, Suji
Yoo, Seungjong
Kim, Hyunzu
Hee Jung, Kyung
Hong, Soon-Sun
description •Anesthetics have a potential impact on the long-term tumor growth, metastasis risk, and recurrence of cancer patients after surgery.•Lidocaine combined with general anesthetics inhibits the metastasis and recurrence of breast cancer by blocking EMT signaling.•Lidocaine not only reduced M2-tumor-associated macrophages (TAM), but also increased macrophage M1 polarization in TNBC.•The combined anesthetics may offer a therapeutic approach to prevent breast cancer recurrence and metastasis in patients after curative resection. Surgical resection is the best-known approach for breast cancer treatment. However, post-operative metastases increase the rate of death. The potential effect of anesthetic drugs on long-term tumor growth, risk of metastasis, and recurrence after surgery has been investigated in cancer patients. However, the underlying mechanisms remain unclear. Therefore, we aimed to elucidate the anti-metastatic effect of lidocaine combined with common anesthetics and its mechanisms of action on lung metastasis in breast cancer models. The combination of lidocaine with propofol or sevoflurane inhibited the growth of TNBC cells compared to treatment alone. In addition, the combination effectively inhibited cancer cell migration and invasion. It suppressed tumor growth and increased the survival rate in breast 4 T1 orthotopic models. More importantly, it inhibited lung metastasis and recurrence compared with groups treated with a single anesthetic. In co-culture with TAMs and TNBC cells, lidocaine not only reduced M2-tumor-associated macrophages (TAM) that were increased by sevoflurane or propofol but also increased M1 macrophage polarization, impeding tumor growth in TNBC. Also, we found that the transforming growth factor-β (TGF-β) derived from TAMs increased EMT signaling in TNBC cells, and that lidocaine affected cancer cells as well as M2-TAMs, inducing M2 to M1 reprogramming and decreasing TGF-β/Smads-mediated EMT signaling in TNBC cells, leading to inhibition of cancer metastasis and recurrence. These findings suggest lidocaine combined with general anesthetics as a potential therapeutic approach for the inhibition of recurrence and metastasis of breast cancer patients undergoing curative resection.
doi_str_mv 10.1016/j.intimp.2024.113207
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Surgical resection is the best-known approach for breast cancer treatment. However, post-operative metastases increase the rate of death. The potential effect of anesthetic drugs on long-term tumor growth, risk of metastasis, and recurrence after surgery has been investigated in cancer patients. However, the underlying mechanisms remain unclear. Therefore, we aimed to elucidate the anti-metastatic effect of lidocaine combined with common anesthetics and its mechanisms of action on lung metastasis in breast cancer models. The combination of lidocaine with propofol or sevoflurane inhibited the growth of TNBC cells compared to treatment alone. In addition, the combination effectively inhibited cancer cell migration and invasion. It suppressed tumor growth and increased the survival rate in breast 4 T1 orthotopic models. More importantly, it inhibited lung metastasis and recurrence compared with groups treated with a single anesthetic. In co-culture with TAMs and TNBC cells, lidocaine not only reduced M2-tumor-associated macrophages (TAM) that were increased by sevoflurane or propofol but also increased M1 macrophage polarization, impeding tumor growth in TNBC. Also, we found that the transforming growth factor-β (TGF-β) derived from TAMs increased EMT signaling in TNBC cells, and that lidocaine affected cancer cells as well as M2-TAMs, inducing M2 to M1 reprogramming and decreasing TGF-β/Smads-mediated EMT signaling in TNBC cells, leading to inhibition of cancer metastasis and recurrence. 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Surgical resection is the best-known approach for breast cancer treatment. However, post-operative metastases increase the rate of death. The potential effect of anesthetic drugs on long-term tumor growth, risk of metastasis, and recurrence after surgery has been investigated in cancer patients. However, the underlying mechanisms remain unclear. Therefore, we aimed to elucidate the anti-metastatic effect of lidocaine combined with common anesthetics and its mechanisms of action on lung metastasis in breast cancer models. The combination of lidocaine with propofol or sevoflurane inhibited the growth of TNBC cells compared to treatment alone. In addition, the combination effectively inhibited cancer cell migration and invasion. It suppressed tumor growth and increased the survival rate in breast 4 T1 orthotopic models. More importantly, it inhibited lung metastasis and recurrence compared with groups treated with a single anesthetic. 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subjects Breast cancer
EMT pathway
General anesthetics
Lidocaine
TAM
title Lidocaine combined with general anesthetics impedes metastasis of breast cancer cells via inhibition of TGF-β/Smad-mediated EMT signaling by reprogramming tumor-associated macrophages
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