African Journal of
Biotechnology

  • Abbreviation: Afr. J. Biotechnol.
  • Language: English
  • ISSN: 1684-5315
  • DOI: 10.5897/AJB
  • Start Year: 2002
  • Published Articles: 12487

Review

From HAMLET to XAMLET: The molecular complex selectively induces cancer cell death

  Yi-Bo Zhang1, Wei Wu2* and Wei Ding1*  
1Department of Biochemistry and Molecular Biology, School of Basic Medical Sciences, Capital Medical University, Beijing 100069, People’s Republic of China. 2Department of Epidemiology and Health Statistics, School of Public Health and Family Medicine, Capital Medical University, Beijing 100069, People’s Republic of China.
Email: [email protected], [email protected]

  •  Accepted: 27 December 2010
  •  Published: 29 December 2010

Abstract

 

HAMLET (human α-lactalbumin made lethal to tumor cells) is a complex consisting of decalcinated α-lactalbumin and oleic acid. It has been shown to induce massive cell death in various cancers without serious damage to normal tissues in both in vitro and in vivo experiments. The complexity of the mechanism in the cellular functions of HAMLET results from its heterogeneous compositions as revealed from the structural analyses, as well as its induction of the non-canonical cell responses different from the specific classical programmed cell death. As the remarkable progress was made in the studies of HAMLET in recent years, a variety of HAMLET-like substances have been demonstrated to exert similar biological activities to HAMLET. Here, we termed these species as the XAMLET, and overviewed the current findings in XAMLET studies for a better understanding of their functions and working mechanisms. This review might contribute to the improvement in the application of XAMLET towards clinical cancer therapies.

 

Key words: XAMLET, α-lactalbumin, cancer cell death.

Abbreviation

Abbreviations: HAMLET, Human α-lactalbumin made lethal to tumor cells; MAL, multimeric α-lactalbumin; α-LA, α-lactalbumin; OA, oleic acid; HLA, human α-lactalbumin; PI3K, phosphoinositide 3-kinase; LC3, light chain 3; Atg8, autophagy-related gene 8.