Journals / Türk Biyokimya Dergisi / 2019 / Cilt: 44 - Sayı: 6

Effects of α-lactalbumin and sulindac on primary and metastatic human colon cancer cell lines

Sulindac ve α-laktalbuminin primer ve metastatik insan kolon kanseri hücre dizinleri üzerine etkileri

Pages
787–796
Publication Date
2022-11-04
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In our study, we aimed toinvestigate effects of α-lactalbumin and sulindac on COLO320 primary and COLO-741 metastatic human colon carcinoma cell lines via mitochondrial apoptotic pathway byindirect immunocytochemistry and TUNEL assays.Materials and methods: The effects of α-lactalbuminand sulindac were assessed by using MTT assay at 24, 48and 72 h and apoptosis markers caspase-3, caspase-9 andcytochrome-c were detected using immunocytochemistryand TUNEL methods.Results: It was appeared that α-lactalbumin and sulindacmay triggger mechanisms of apoptosis in both primaryand metastatic colon carcinoma cell lines and the primarycolon carcinoma cell line was affected more than the metastatic cells.Conclusion: It is proposed that α-lactalbumin and sulindac can be used in cancer treatments and future in vivoexperiments.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Background: HAMLET (human α-lactalbumin made lethalto tumor cells) and sulindac are active ingredients whichare used in the treatment of cancers.
📊
Key Findings & Data:Under both in vivo andin vitro conditions, HAMLET binds to the surface of tumorcells and enters the cells.
💡
Conclusion & Impact:In our study, we aimed toinvestigate effects of α-lactalbumin and sulindac on COLO320 primary and COLO-741 metastatic human colon carcinoma cell lines via mitochondrial apoptotic pathway byindirect immunocytochemistry and TUNEL assays.Materials and methods: The effects of α-lactalbuminand sulindac were assessed by using MTT assay at 24, 48and 72 h and apoptosis markers caspase-3, caspase-9 andcytochrome-c were detected using immunocytochemistryand TUNEL methods.Results: It was appeared that α-lactalbumin and sulindacmay triggger mechanisms of apoptosis in both primaryand metastatic colon carcinoma cell lines and the primarycolon carcinoma cell line was affected more than the metastatic cells.Conclusion: It is proposed that α-lactalbumin and sulindac can be used in cancer treatments and future in vivoexperiments.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Background: HAMLET (human α-lactalbumin made lethalto tumor cells) and sulindac are active ingredients whichare used in the treatment of cancers. Under both in vivo andin vitro conditions, HAMLET binds to the surface of tumorcells and enters the cells. Sulindac is one of nonsteroidalanti-inflammatory drugs. It inhibits the growth of tumorcells by inducing the apoptosis. In our study, we aimed toinvestigate effects of α-lactalbumin and sulindac on COLO320 primary and COLO-741 metastatic human colon carcinoma cell lines via mitochondrial apoptotic pathway byindirect immunocytochemistry and TUNEL assays.Materials and methods: The effects of α-lactalbuminand sulindac were assessed by using MTT assay at 24, 48and 72 h and apoptosis markers caspase-3, caspase-9 andcytochrome-c were detected using immunocytochemistryand TUNEL methods.Results: It was appeared that α-lactalbumin and sulindacmay triggger mechanisms of apoptosis in both primaryand metastatic colon carcinoma cell lines and the primarycolon carcinoma cell line was affected more than the metastatic cells.Conclusion: It is proposed that α-lactalbumin and sulindac can be used in cancer treatments and future in vivoexperiments.

Özet

Amaç: HAMLET (human α-lactalbumin made lethal to tumor cells) ve sulindac, kanser tedavisinde kullanılan etken maddelerdir. HAMLET, in vivo ve in vitro koşullar altında, tümör hücrelerinin yüzeyine bağlanarak hücre içerisine girer. Sulindac, non-steroidal bir anti-inflamatuvar ilaçlardan biridir ve apoptozu tetikleyerek tümör hücrelerinin çoğalmasını inhibe eder. Çalışmamızda α-laktalbumin ve sulindac’ın COLO-320 primer ve COLO741 metastatik insan kolon karsinomu hücre dizinleri üzerindeki etkilerini, mitokondriyal apoptotik yolak aracılığı ile immünositokimya ve TUNEL yöntemleri ile araştırmayı amaçladık. Gereç ve Yöntem: Sulindac ve α-laktalbuminin etkileri 24, 48 ve 72. saatlerde MTT metodu ile değerlendirildi ve immünositokimyasal olarak apoptoz belirteçleri kaspaz3, kaspaz-9 ve sitokrom-c, ve TUNEL boyama yöntemleri uygulandı. Bulgular: Sulindac ve α-laktalbuminin hem primer hem de metastatik kolon karsinoma hücrelerinde apoptoz mekanizmalarını tetikleyebileceği ve primer kolon karsinom hücrelerinin, metastatik hücrelerden daha fazla etkilendiği saptandı. Sonuç: Sulindac ve α-laktalbuminin, gelecekte in vivo çalışmalarda ve kanser tedavilerinde kullanılabileceği düşünülmektedir.

🔖

Cite This Article

ÖZBİLGİN, K., VATANSEVER, S., AYDEMİR, I. (2022). Effects of α-lactalbumin and sulindac on primary and metastatic human colon cancer cell lines. Türk Biyokimya Dergisi, Cilt: 44 - Sayı: 6, 787–796. https://ajindex.com/articles/620881

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (13)

  1. Jemal A, Center MM, DeSantis C, Ward EM. Global patterns of cancer incidence and mortality rates and trends. Cancer Epidemiol Biomarkers Prev 2010;19:1893–907
  2. Dai L, Wang W, Zhang S, Jiang Q, Wang R, Dai L, et al. Vectorbased miR-15a/16-1 plasmid inhibits colon cancer growth in vivo. Cell Biol Int 2012;36:765–70
  3. Hyodo I, Suzuki H, Takahashi K, Saito Y, Tanaka S, Chiu HM, et al. Present status and perspectives of colorectal cancer in Asia: Colorectal Cancer Working Group report in 30th AsiaPacific Cancer Conference. Jpn J Clin Oncol 2010;40(Suppl1):i38–43
  4. Aitini E, Rossi A, Morselli P, Vivorio B, Bruschi A, Bottura C, et al. Economic comparison of capecitabine + oxaliplatin and 5-fluorouracil + oxaliplatin in the adjuvant treatment of colon cancer. Cancer Manag Res 2012;4:99–103
  5. Puthia M, Storm P, Nadeem A, Hsiung S, Svanborg C. Prevention and treatment of colon cancer by peroral administration of HAMLET (human α-lactalbumin made lethal to tumour cells). Gut 2014;63:131–42
  6. Horinaka M, Yoshida T, Tomosugi M, Yasuda S, Sowa Y, Sakai T. Myeloid zinc finger 1 mediates sulindac sulfide-induced upregulation of death receptor 5 of human colon cancer cells. Sci Rep 2014;4:6000
  7. Ho J, Sielaff H, Nadeem A, Svanborg C, Grüber G. The molecular motor F-ATP synthase is targeted by the tumoricidal protein HAMLET. J Mol Biol 2015;427:1866–74
  8. Permyakov SE, Knyazeva EL, Leonteva MV, Fadeev RS, Chekanov AV, Zhadan AP, et al. A novel method for preparation of HAMLET-like protein complexes. Biochimie 2011;93: 1495–501
  9. Düringer C, Hamiche A, Gustafsson L, Kimura H, Svanborg C. HAMLET interacts with histones and chromatin in tumor cell nuclei. J Biol Chem 2003;278:42131–5
  10. Rath EM, Duff AP, Håkansson AP, Vacher CS, Liu GJ, Knott RB, et al. Structure and potential cellular targets of HAMLET-like anti-cancer compounds made from milk components. J Pharm Pharm Sci 2015;18:773–824
  11. Piazza GA, Rahm AK, Finn TS, Fryer BH, Li H, Stoumen AL, et al. Apoptosis primarily accounts for the growth-inhibitory properties of sulindac metabolites and involves a mechanism that is independent of cyclooxygenase inhibition, cell cycle arrest, and p53 induction. Cancer Res 1997;57:2452–9
  12. Mladenova D, Pangon L, Currey N, Ng I, Musgrove EA, Grey ST, et al. Sulindac activates NF-κB signaling in colon cancer cells. Cell Commun Signal 2013;11:73
  13. Nortcliffe A, Ekstrom AG, Black JR, Ross JA, Habib FK, Botting NP, et al. Synthesis and biological evaluation of