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Effect of lidocaine and ropivacaine on primary (SW480) and metastatic (SW620) colon cancer cell lines
Örebro University, School of Medical Sciences. Department of Anesthesiology and Intensive Care.
Örebro University, School of Medical Sciences. Department of Clinical Research Laboratory,.
Örebro University, School of Medical Sciences. Department of Clinical Research Laboratory.ORCID iD: 0000-0001-8304-2772
Department of Physiology and Pharmacology, Karolinska Institute and Karolinska University Hospital, Stockholm; School of Medical Sciences, Örebro University, Örebro, Sweden.
2019 (English)In: Oncology Letters, ISSN 1792-1074, E-ISSN 1792-1082, Vol. 18, no 1, p. 395-401Article in journal (Refereed) Published
Abstract [en]

Regional anesthesia may prolong survival following surgery for different types of cancers. The mechanisms behind this are unclear but direct effects on cancer cells by local anesthetics (LA) have been suggested. The aim of this study was to investigate if lidocaine or ropivacaine have a dose-dependent effect on the cell viability and proliferation of a primary and a secondary colon carcinoma cell line in vitro. The colon cancer cell lines SW480 derived from primary tumor and SW620 from a metastatic site in the same patient were exposed to increasing concentrations of lidocaine and ropivacaine (5-1,000 mu M). Cell viability was measured using CellTiter-Blue((R)) and cell proliferation by PKH67 after exposure for up to 72 h. Cell viability was significantly reduced by ropivacaine at the highest concentration (1,000 mu M) after 48 and 72 h in the cell line SW480 and at 72 h in SW620. Exposure to lidocaine did not show any significant reduction in cell viability. Notably, low concentrations of both lidocaine and ropivacaine significantly increased cell viability after 48 and 72 h in SW620. Cell proliferation was significantly reduced by 1,000 mu M lidocaine in SW480 and by 1,000 mu M ropivacaine in SW620. In summary, both lidocaine and ropivacaine showed an anti-proliferative effect in the colon cancer cell lines at high concentrations and after prolonged exposure to LA in vitro. Our findings also indicate that lower concentrations promote cell viability in the metastatic cell line.

Place, publisher, year, edition, pages
Spandidos Publications , 2019. Vol. 18, no 1, p. 395-401
Keywords [en]
local anesthetics, colon cancer, SW480, SW620, in vitro, cell viability, proliferation
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:oru:diva-75408DOI: 10.3892/ol.2019.10332ISI: 000474896900047Scopus ID: 2-s2.0-85068799738OAI: oai:DiVA.org:oru-75408DiVA, id: diva2:1339562
Note

Funding Agency:

Research Committee of the Örebro County Council

Available from: 2019-07-30 Created: 2019-07-30 Last updated: 2021-05-10Bibliographically approved
In thesis
1. Epidural Analgesia for Colorectal Cancer Surgery: Experimental and Clinical studies
Open this publication in new window or tab >>Epidural Analgesia for Colorectal Cancer Surgery: Experimental and Clinical studies
2021 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Epidural analgesia (EA) with local anaesthetics and opioids is used for pain management after colorectal cancer (CRC) surgery. In recent years, a possible beneficial effect of EA on cancer recurrence and survival after surgery has been proposed. The aim of this thesis was to study the effects of EA on short- and long-term postoperative outcomes after CRC surgery with curative intent.

Study I, an in vitro study, investigated the effects of two different local anaesthetics, lidocaine and ropivacaine, on cell viability and cell proliferation in colon cancer cell lines SW480 and SW620. Neither lidocaine nor ropivacaine reduced cell viability or proliferation at systemically, by epidural administration achievable concentrations.

In study II, the effect of EA on the systemic level of different cytokines as a marker of inflammation was studied. Except for a reduced level of the anti-inflammatory cytokine IL-10, no other significant effects of EA on the systemic cytokine levels at two time points postoperatively could be shown, when compared to patients receiving intravenous morphine.

Study III was an epidemiological study, examining the question if EA affects postoperative complications and mortality after surgery using data from the Swedish Colorectal Cancer Registry and the Swedish Perioperative Registry. No association between EA and a reduction in postoperative complications or mortality could be established.

Study IV, a randomised, controlled trial, the effects of EA on diseasefree survival (DFS), postoperative complications and pain after surgery were compared to patient-controlled intravenous analgesia with morphine. Apart from superior pain relief during the first postoperative day, no significant effects of EA on the occurrence of postoperative complications, length of hospital stay or DFS were found.

Place, publisher, year, edition, pages
Örebro: Örebro University, 2021. p. 67
Series
Örebro Studies in Medicine, ISSN 1652-4063 ; 237
Keywords
colorectal cancer, epidural analgesia, local anaesthetics, colon cancer cells, inflammation, postoperative complications, pain, recurrence, disease-free survival, mortality
National Category
Surgery
Identifiers
urn:nbn:se:oru:diva-90317 (URN)978-91-7529-384-4 (ISBN)
Public defence
2021-06-03, Örebro universitet, Campus USÖ, hörsal C1, Södra Grev Rosengatan 32, Örebro, 09:00 (Swedish)
Opponent
Supervisors
Available from: 2021-03-09 Created: 2021-03-09 Last updated: 2022-02-11Bibliographically approved

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Siekmann, WiebkeTina, ElisabetKoskela von Sydow, Anita

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