Plasmalemmal V-ATPase as a Potential Biomarker for Lactoferrin-Based Anticancer Therapy

被引:7
作者
Santos-Pereira, Catia [1 ,2 ]
Rodrigues, Ligia R. [2 ]
Corte-Real, Manuela [1 ]
机构
[1] Univ Minho, Dept Biol, Ctr Mol & Environm Biol CBMA, P-4710057 Braga, Portugal
[2] Univ Minho, Dept Biol Engn, Ctr Biol Engn CEB, P-4710057 Braga, Portugal
关键词
biomarker; cancer; lactoferrin; V-ATPase; BOVINE LACTOFERRIN; LUNG-CANCER; IN-VIVO; NASOPHARYNGEAL CARCINOMA; ORAL TALACTOFERRIN; TUMOR-SUPPRESSOR; EXPRESSION; LACTOTRANSFERRIN; GROWTH; PROTEIN;
D O I
10.3390/biom12010119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Lactoferrin (Lf) is a milk-derived protein with well-recognized potential as a therapeutic agent against a wide variety of cancers. This natural protein exhibits health-promoting effects and has several interesting features, including its selectivity towards cancer cells, good tolerability in humans, worldwide availability, and holding a generally recognized as safe (GRAS) status. To prompt the rational clinical application of this promising anticancer compound, previous works aimed to unveil the molecular mechanisms underlying its selective anticancer activity, where plasmalemmal V-ATPase was identified as an Lf target in cancer cells. V-ATPase is a proton pump critical for cellular homeostasis that migrates to the plasma membrane of highly metastatic cancer cells contributing to the acidity of the tumor microenvironment. Cancer cells were found to be susceptible to Lf only when this proton pump is present at the plasma membrane. Plasmalemmal V-ATPase can thus be an excellent biomarker for driving treatment decisions and forecasting clinical outcomes of Lf-based anticancer strategies. Future research endeavors should thus seek to validate this biomarker by thorough preclinical and clinical studies, as well as to develop effective methods for its detection under clinical settings.
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页数:9
相关论文
共 62 条
[1]   Development of Encapsulation Strategies and Composite Edible Films to Maintain Lactoferrin Bioactivity: A Review [J].
Abad, Ines ;
Conesa, Celia ;
Sanchez, Lourdes .
MATERIALS, 2021, 14 (23)
[2]   Inhalable Lactoferrin/Chondroitin-Functionalized Monoolein Nanocomposites for Localized Lung Cancer Targeting [J].
Abdelaziz, Hadeer M. ;
Elzoghby, Ahmed O. ;
Helmy, Maged W. ;
Abdelfattah, Elsayeda-Zeinab A. ;
Fang, Jia-You ;
Samaha, Magda W. ;
Freag, May S. .
ACS BIOMATERIALS SCIENCE & ENGINEERING, 2020, 6 (02) :1030-1042
[4]   In vitro and in vivo effect of human lactoferrin on glioblastoma growth [J].
Arcella, Antonietta ;
Oliva, Maria Antonietta ;
Staffieri, Sabrina ;
Alberti, Silvia ;
Grillea, Giovanni ;
Madonna, Michele ;
Bartolo, Marcello ;
Pavone, Luigi ;
Giangaspero, Felice ;
Cantore, Giampaolo ;
Frati, Alessandro .
JOURNAL OF NEUROSURGERY, 2015, 123 (04) :1026-1035
[5]  
Aronson Jeffrey K, 2017, Curr Protoc Pharmacol, V76, DOI 10.1002/cpph.19
[6]  
BEZAULT J, 1994, CANCER RES, V54, P2310
[7]   Bovine lactoferrin reverses programming of epithelial-to-mesenchymal transition to mesenchymal-to-epithelial transition in oral squamous cell carcinoma [J].
Chea, Chanbora ;
Miyauchi, Mutsumi ;
Inubushi, Toshihiro ;
Okamoto, Kana ;
Haing, Sivmeng ;
Phuong Thao Nguyen ;
Imanaka, Hiromichi ;
Takata, Takashi .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 507 (1-4) :142-147
[8]   Molecular mechanism of inhibitory effects of bovine lactoferrin on the growth of oral squamous cell carcinoma [J].
Chea, Chanbora ;
Miyauchi, Mutsumi ;
Inubushi, Toshihiro ;
Ayuningtyas, Nurina Febriyanti ;
Subarnbhesaj, Ajiravudh ;
Phuong Thao Nguyen ;
Shrestha, Madhu ;
Haing, Sivmeng ;
Ohta, Kouji ;
Takata, Takashi .
PLOS ONE, 2018, 13 (01)
[9]   Lactoferrin's Anti-Cancer Properties: Safety, Selectivity, and Wide Range of Action [J].
Cutone, Antimo ;
Rosa, Luigi ;
Ianiro, Giusi ;
Lepanto, Maria Stefania ;
di Patti, Maria Carmela Bonaccorsi ;
Valenti, Piera ;
Musci, Giovanni .
BIOMOLECULES, 2020, 10 (03)
[10]   Native and iron-saturated bovine lactoferrin differently hinder migration in a model of human glioblastoma by reverting epithelial-to-mesenchymal transition-like process and inhibiting interleukin-6/STAT3 axis [J].
Cutone, Antimo ;
Colella, Barbara ;
Pagliaro, Andrea ;
Rosa, Luigi ;
Lepanto, Maria Stefania ;
di Patti, Maria Carmela Bonaccorsi ;
Valenti, Piera ;
Di Bartolomeo, Sabrina ;
Musci, Giovanni .
CELLULAR SIGNALLING, 2020, 65