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Wahab MF, Breitbach ZS, Armstrong DW, Strattan R, Berthod A. Problems and pitfalls in the analysis of amygdalin and its epimer. J Agric Food Chem. 2015; 63: 8966–8973. WahabMF BreitbachZS ArmstrongDW StrattanR BerthodA Problems and pitfalls in the analysis of amygdalin and its epimer J Agric Food Chem 2015 63 8966 8973 10.1021/acs.jafc.5b0312026431391 Search in Google Scholar

Blaheta RA, Nelsonb K, Haferkampa A, Juengela E. Amygdalin, quackery or cure? Phytomedicine. 2016; 23: 367–376. BlahetaRA NelsonbK HaferkampaA JuengelaE Amygdalin, quackery or cure? Phytomedicine 2016 23 367 376 10.1016/j.phymed.2016.02.00427002407 Search in Google Scholar

Unproven methods of cancer management. Laetrile. CA: Cancer J Clin. 1991; 41: 187–192. Unproven methods of cancer management Laetrile. CA: Cancer J Clin 1991 41 187 192 Search in Google Scholar

Laetrile/Amygdalin: PDQ Cancer Complementary and Alternative Medicine Editorial Board, 2019. http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0032851/ (05.11.2020). Laetrile/Amygdalin PDQ Cancer Complementary and Alternative Medicine Editorial Board 2019 http://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0032851/ (05.11.2020). Search in Google Scholar

Zuoqing S, Xiaohong X. Advanced research on anti-tumor effects of amygdalin. J Cancer Res Ther. 2014; 10 (Special Issue): C3–C7. ZuoqingS XiaohongX Advanced research on anti-tumor effects of amygdalin J Cancer Res Ther 2014 10 Special Issue C3 C7 10.4103/0973-1482.13974325207888 Search in Google Scholar

Newmark J, Brady RO, Grimley PM, Gal AE, Waller SG, Thistlethwaite JR. Amygdalin (laetrile) and prunasin beta-glucosidases: Distribution in germ-free rat and in human tumor tissue. Proc Natl Acad Sci USA. 1981; 78: 6513–6516. NewmarkJ BradyRO GrimleyPM GalAE WallerSG ThistlethwaiteJR Amygdalin (laetrile) and prunasin beta-glucosidases: Distribution in germ-free rat and in human tumor tissue Proc Natl Acad Sci USA 1981 78 6513 6516 10.1073/pnas.78.10.65133490706796962 Search in Google Scholar

Abboud MM, Al Awaida W, Alkhateeb HH, Abu-Ayyad AN. Antitumor action of amygdalin on human breast cancer cells by selective sensitization to oxidative stress. Nutr Cancer. 2019; 71: 483–490. AbboudMM Al AwaidaW AlkhateebHH Abu-AyyadAN Antitumor action of amygdalin on human breast cancer cells by selective sensitization to oxidative stress Nutr Cancer 2019 71 483 490 10.1080/01635581.2018.150873130407870 Search in Google Scholar

Chang HK, Shin MS, Yang HY, Lee JW, Kim YS, Lee MH, Kim J, Kim KH, Kim CJ. Amygdalin induces apoptosis through regulation of Bax and Bcl-2 expressions in human DU145 and LNCaP prostate cancer cells. Biol Pharm Bull. 2006; 29: 1597–1602. ChangHK ShinMS YangHY LeeJW KimYS LeeMH KimJ KimKH KimCJ Amygdalin induces apoptosis through regulation of Bax and Bcl-2 expressions in human DU145 and LNCaP prostate cancer cells Biol Pharm Bull 2006 29 1597 1602 10.1248/bpb.29.159716880611 Search in Google Scholar

Milazzo S, Lejeune S, Ernst E. Laetrile for cancer: A systematic review of the clinical evidence. Support Care Cancer. 2007; 15: 583–595. MilazzoS LejeuneS ErnstE Laetrile for cancer: A systematic review of the clinical evidence Support Care Cancer 2007 15 583 595 10.1007/s00520-006-0168-917106659 Search in Google Scholar

Kim YS, Kim JJ, Cho KH, Jung WS, Moon SK, Park EK, Kim DH. Biotrans-formation of ginsenoside Rb1, crocin, amygdalin, geniposide, puerarin, ginsenoside Re, hesperidin, poncirin, glycyrrhizin, and baicalin by human fecal microflora and its relation to cytotoxicity against tumor cells. J Microbiol Biotechnol. 2008; 18: 1109–1114. KimYS KimJJ ChoKH JungWS MoonSK ParkEK KimDH Biotrans-formation of ginsenoside Rb1, crocin, amygdalin, geniposide, puerarin, ginsenoside Re, hesperidin, poncirin, glycyrrhizin, and baicalin by human fecal microflora and its relation to cytotoxicity against tumor cells J Microbiol Biotechnol 2008 18 1109 1114 Search in Google Scholar

Song Z, Xu X. Advanced research on anti-tumor effects of amygdalin. J Cancer Res Ther. 2014; 10 (Suppl 1): 3–7. SongZ XuX Advanced research on anti-tumor effects of amygdalin J Cancer Res Ther 2014 10 Suppl 1 3 7 10.4103/0973-1482.139743 Search in Google Scholar

Park HJ, Yoon SH, Han LS, Zheng LT, Jung KH, Uhm YK, Lee JH, Jeong JS, Joo WS, Yim SV, et al. Amygdalin inhibits genes related to cell cycle in SNU-C4 human colon cancer cells. World J Gastroenterol. 2005; 11: 5156–5161. ParkHJ YoonSH HanLS ZhengLT JungKH UhmYK LeeJH JeongJS JooWS YimSV Amygdalin inhibits genes related to cell cycle in SNU-C4 human colon cancer cells World J Gastroenterol 2005 11 5156 5161 Search in Google Scholar

Makarevic J, Rutz J, Juengel E, Kaulfuss S, Reiter M, Tsaur I, Bartsch G, Haferkamp A, Roman A, Blaheta RA. Amygdalin blocks bladder cancer cell growth in vitro by diminishing cyclin A and cdk2. PLoS One. 2014; 9: 105590. MakarevicJ RutzJ JuengelE KaulfussS ReiterM TsaurI BartschG HaferkampA RomanA BlahetaRA Amygdalin blocks bladder cancer cell growth in vitro by diminishing cyclin A and cdk2 PLoS One 2014 9 105590 10.1371/journal.pone.0105590413818925136960 Search in Google Scholar

Kwon HY, Hong SP, Hahn DH, Kim JH. Apoptosis induction of Persicae semen extract in human promyelocytic leukemia (HL-60) cells. Arch Pharm Res. 2003; 26: 157–161. KwonHY HongSP HahnDH KimJH Apoptosis induction of Persicae semen extract in human promyelocytic leukemia (HL-60) cells Arch Pharm Res 2003 26 157 161 10.1007/BF0297666312643594 Search in Google Scholar

Makarević J, Rutz J, Juengel E, Kaulfuss S, Reiter M, Tsaur I, Bartsch G, Haferkamp A. Blaheta RA. Amygdalin blocks bladder cancer cell growth in vitro by diminishing cyclin A and cdk2. PLoS One, 2014; 9: e10559.0. MakarevićJ RutzJ JuengelE KaulfussS ReiterM TsaurI BartschG HaferkampA BlahetaRA Amygdalin blocks bladder cancer cell growth in vitro by diminishing cyclin A and cdk2 PLoS One 2014 9 e10559.0 10.1371/journal.pone.0105590413818925136960 Search in Google Scholar

Lee HM, Moon A. Amygdalin regulates apoptosis and adhesion in Hs578T triple-negative breast cancer cells. Biomol Ther. 2016; 24: 62–66. LeeHM MoonA Amygdalin regulates apoptosis and adhesion in Hs578T triple-negative breast cancer cells Biomol Ther 2016 24 62 66 10.4062/biomolther.2015.172470335426759703 Search in Google Scholar

Moradipoodeh B, Jamalan M, Zeinali M, Fereidoonnezhad M, Mohammadzadeh G. In vitro and in silico anticancer activity of amygdalin on the SK-BR-3 human breast cancer cell line. Mol Biol Rep. 2019; 46: 6361–6370. MoradipoodehB JamalanM ZeinaliM FereidoonnezhadM MohammadzadehG In vitro and in silico anticancer activity of amygdalin on the SK-BR-3 human breast cancer cell line Mol Biol Rep 2019 46 6361 6370 10.1007/s11033-019-05080-331583572 Search in Google Scholar

Qian L, Xie B, Wang Y, Qian J. Amygdalin-mediated inhibition of non-small cell lung cancer cell invasion in vitro. Int J Clin Exp Pathol. 2015; 8: 5363–5370. QianL XieB WangY QianJ Amygdalin-mediated inhibition of non-small cell lung cancer cell invasion in vitro Int J Clin Exp Pathol 2015 8 5363 5370 Search in Google Scholar

Chen Y, Ma J, Wang F, Hu J, Cui A, Wei C, Yang Q, Li F. Amygdalin induces apoptosis in human cervical cancer cell line HeLa cells. Immunopharm Immunot. 2013; 35: 43–51. ChenY MaJ WangF HuJ CuiA WeiC YangQ LiF Amygdalin induces apoptosis in human cervical cancer cell line HeLa cells Immunopharm Immunot 2013 35 43 51 10.3109/08923973.2012.73868823137229 Search in Google Scholar

Elemore S. Apoptosis: A revive of programmed cell death. Toxicol Pathol. 2007; 35: 495–516. ElemoreS Apoptosis: A revive of programmed cell death Toxicol Pathol 2007 35 495 516 10.1080/01926230701320337211790317562483 Search in Google Scholar

Hardwick JM, Soane L. Multiple functions of BCL-2 family proteins. Cold Spring Harb Perspect Biol. 2013; 5: a008722. HardwickJM SoaneL Multiple functions of BCL-2 family proteins Cold Spring Harb Perspect Biol 2013 5 a008722 10.1101/cshperspect.a008722355250023378584 Search in Google Scholar

Kale J, Osterlund EJ, Andrews DA. BCL-2 family proteins: changing partners in the dance towards death. Cell Death Differ. 2018; 25: 65–80. KaleJ OsterlundEJ AndrewsDA BCL-2 family proteins: changing partners in the dance towards death Cell Death Differ 2018 25 65 80 10.1038/cdd.2017.186572954029149100 Search in Google Scholar

Saleem M, Asif J, Asif M, Saleem U. Amygdalin from apricot kernels induces and causec cell cycle arrest in cancer cells: An update review. Anticancer Agents Med Chem. 2018; 18: 1–6. SaleemM AsifJ AsifM SaleemU Amygdalin from apricot kernels induces and causec cell cycle arrest in cancer cells: An update review Anticancer Agents Med Chem 2018 18 1 6 Search in Google Scholar

Eguchi H, Suga K, Saji H, Toi M, Nakachi K, Hayashi SI. Different expression patterns of Bcl-2 family genes in breast cancer by estrogen receptor status with special reference to pro-apoptotic Bak gene. Cell Death Differ. 2000; 7: 439–446. EguchiH SugaK SajiH ToiM NakachiK HayashiSI Different expression patterns of Bcl-2 family genes in breast cancer by estrogen receptor status with special reference to pro-apoptotic Bak gene Cell Death Differ 2000 7 439 446 10.1038/sj.cdd.440067510800077 Search in Google Scholar

McIlwain DR, Berger T, Mak TW. Caspase functions in cell death and disease. Cold Spring Harb Perspect Biol. 2015; 7: a026716. McIlwainDR BergerT MakTW Caspase functions in cell death and disease Cold Spring Harb Perspect Biol 2015 7 a026716 10.1101/cshperspect.a008656368389623545416 Search in Google Scholar

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