Literature DB >> 24393556

Alkylphospholipids - a promising class of chemotherapeutic agents with a broad pharmacological spectrum.

Juliana de Almeida Pachioni1, Juliana Gallottini Magalhães, Elys Juliane Cardoso Lima, Luciana de Moura Bueno, Joyce Ferreira Barbosa, Matheus Malta de Sá, Carlota Oliveira Rangel-Yagui.   

Abstract

PURPOSE: Since when alkylphospholipds (ALPs) were discovered and, even further after miltefosine's approval for the treatment of cutaneous metastasis of breast cancer and leishmaniasis, their activity against many other diseases have been extensively studied. This review aims to provide a summary of the alkylphospholipids' applications investigated so far.
RESULTS: The mechanism of action of ALPs is not fully understood, however it is believed that they interfere with lipid homeostasis leading to cell apoptosis. Due to ALPs cytotoxic activity, this class of molecules has shown to be effective against many diseases and conditions. Besides the approval of miltefosine for application in cutaneous metastasis of breast cancer and visceral and cutaneous leishmaniasis, several other analogs have proved efficacy and are promising as less toxic alternatives. ALPs have also shown in vitro and in vivo activity against Trypanosoma spp., amoebae, Tricomonas vaginalis, Schistosoma mansoni, HIV, and some fungi and bacteria species. The use of ALPs for intraocular lens coating is also under investigation. In addition, a clinical trial comparing miltefosine with usual treatments to spontaneous urticaria is also being conducted.
CONCLUSIONS: Alkylphospholipids present such a broad pharmacological spectrum that justifies the need for further investigations of the drug class mechanisms of action, as well as the search for new analogs with improved activity and toxicological profiles.

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Year:  2013        PMID: 24393556     DOI: 10.18433/j3cw23

Source DB:  PubMed          Journal:  J Pharm Pharm Sci        ISSN: 1482-1826            Impact factor:   2.327


  14 in total

1.  Miltefosine Has a Postantifungal Effect and Induces Apoptosis in Cryptococcus Yeasts.

Authors:  Cristina de Castro Spadari; Taissa Vila; Sonia Rozental; Kelly Ishida
Journal:  Antimicrob Agents Chemother       Date:  2018-07-27       Impact factor: 5.191

2.  Tumor-selective anti-cancer effects of the synthetic alkyl phosphocholine analog CLR1404 in neuroblastoma.

Authors:  Roberta Marino; Dana C Baiu; Saswati Bhattacharya; Benjamin Titz; Ellen Hebron; Bryan D Menapace; Sorabh Singhal; Jens C Eickhoff; Fotis Asimakopoulos; Jamey P Weichert; Mario Otto
Journal:  Am J Cancer Res       Date:  2015-10-15       Impact factor: 6.166

3.  Inhibition of Granulomatous Inflammation and Prophylactic Treatment of Schistosomiasis with a Combination of Edelfosine and Praziquantel.

Authors:  Edward Yepes; Rubén E Varela-M; Julio López-Abán; Jose Rojas-Caraballo; Antonio Muro; Faustino Mollinedo
Journal:  PLoS Negl Trop Dis       Date:  2015-07-20

Review 4.  Akt inhibitors in cancer treatment: The long journey from drug discovery to clinical use (Review).

Authors:  George Mihai Nitulescu; Denisa Margina; Petras Juzenas; Qian Peng; Octavian Tudorel Olaru; Emmanouil Saloustros; Concettina Fenga; Demetrios Α Spandidos; Massimo Libra; Aristidis M Tsatsakis
Journal:  Int J Oncol       Date:  2015-12-24       Impact factor: 5.650

5.  Treatment of Schistosoma mansoni with miltefosine in vitro enhances serological recognition of defined worm surface antigens.

Authors:  Marwa H El-Faham; Maha M Eissa; Joseph E Igetei; Eglal I Amer; Susan Liddell; Mervat Z El-Azzouni; Michael J Doenhoff
Journal:  PLoS Negl Trop Dis       Date:  2017-08-25

6.  Accelerating Drug Discovery Efforts for Trypanosomatidic Infections Using an Integrated Transnational Academic Drug Discovery Platform.

Authors:  Carolina B Moraes; Gesa Witt; Maria Kuzikov; Bernhard Ellinger; Theodora Calogeropoulou; Kyriakos C Prousis; Stefano Mangani; Flavio Di Pisa; Giacomo Landi; Lucia Dello Iacono; Cecilia Pozzi; Lucio H Freitas-Junior; Bruno Dos Santos Pascoalino; Claudia P Bertolacini; Birte Behrens; Oliver Keminer; Jennifer Leu; Markus Wolf; Jeanette Reinshagen; Anabela Cordeiro-da-Silva; Nuno Santarem; Alberto Venturelli; Stephen Wrigley; Deepa Karunakaran; Bethlehem Kebede; Ina Pöhner; Wolfgang Müller; Joanna Panecka-Hofman; Rebecca C Wade; Martina Fenske; Joachim Clos; José María Alunda; María Jesús Corral; Elisa Uliassi; Maria Laura Bolognesi; Pasquale Linciano; Antonio Quotadamo; Stefania Ferrari; Matteo Santucci; Chiara Borsari; Maria Paola Costi; Sheraz Gul
Journal:  SLAS Discov       Date:  2019-03       Impact factor: 3.341

Review 7.  Lipid metabolic reprogramming in cancer cells.

Authors:  S Beloribi-Djefaflia; S Vasseur; F Guillaumond
Journal:  Oncogenesis       Date:  2016-01-25       Impact factor: 7.485

8.  SMYD3-mediated lysine methylation in the PH domain is critical for activation of AKT1.

Authors:  Yuichiro Yoshioka; Takehiro Suzuki; Yo Matsuo; Makoto Nakakido; Giichiro Tsurita; Cristiano Simone; Toshiaki Watanabe; Naoshi Dohmae; Yusuke Nakamura; Ryuji Hamamoto
Journal:  Oncotarget       Date:  2016-11-15

9.  Mast Cell Activation and Microtubule Organization Are Modulated by Miltefosine Through Protein Kinase C Inhibition.

Authors:  Zuzana Rubíková; Vadym Sulimenko; Tomáš Paulenda; Pavel Dráber
Journal:  Front Immunol       Date:  2018-07-09       Impact factor: 7.561

10.  Alginate nanoparticles as non-toxic delivery system for miltefosine in the treatment of candidiasis and cryptococcosis.

Authors:  Cristina de Castro Spadari; Fernanda Walt Mendes da Silva de Bastiani; Luciana Biagini Lopes; Kelly Ishida
Journal:  Int J Nanomedicine       Date:  2019-07-12
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