Ovarian Cancer, Cancer Stem Cells and Current Treatment Strategies: A Potential Role of Magmas in the Current Treatment Methods

被引:54
作者
Ahmed, Nuzhat [1 ,2 ,3 ,4 ]
Kadife, Elif [1 ]
Raza, Ali [1 ,2 ]
Short, Mary [5 ]
Jubinsky, Paul T. [5 ]
Kannourakis, George [1 ,2 ]
机构
[1] Fiona Elsey Canc Res Inst, Ballarat, Vic 3353, Australia
[2] Federat Univ Australia, Ballarat, Vic 3353, Australia
[3] Monash Univ, Ctr Reprod Hlth, Hudson Inst Med Res, Clayton, Vic 3168, Australia
[4] Univ Melbourne, Dept Obstet & Gyanecol, Parkville, Vic 3050, Australia
[5] Albert Einstein Coll Med, Dev & Mol Biol, Bronx, NY 10461 USA
关键词
ovarian cancer; treatment; magmas; EPITHELIAL-MESENCHYMAL TRANSITION; OLAPARIB MAINTENANCE THERAPY; PLATINUM-RESISTANT OVARIAN; PATIENT-DERIVED ORGANOIDS; FOLATE RECEPTOR-ALPHA; FALLOPIAN-TUBE; SURFACE EPITHELIUM; BREAST-CANCER; ALDEHYDE DEHYDROGENASE; INITIATING CELLS;
D O I
10.3390/cells9030719
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epithelial ovarian cancer (EOC) constitutes 90% of ovarian cancers (OC) and is the eighth most common cause of cancer-related death in women. The cancer histologically and genetically is very complex having a high degree of tumour heterogeneity. The pathogenic variability in OC causes significant impediments in effectively treating patients, resulting in a dismal prognosis. Disease progression is predominantly influenced by the peritoneal tumour microenvironment rather than properties of the tumor and is the major contributor to prognosis. Standard treatment of OC patients consists of debulking surgery, followed by chemotherapy, which in most cases end in recurrent chemoresistant disease. This review discusses the different origins of high-grade serous ovarian cancer (HGSOC), the major sub-type of EOC. Tumour heterogeneity, genetic/epigenetic changes, and cancer stem cells (CSC) in facilitating HGSOC progression and their contribution in the circumvention of therapy treatments are included. Several new treatment strategies are discussed including our preliminary proof of concept study describing the role of mitochondria-associated granulocyte macrophage colony-stimulating factor signaling protein (Magmas) in HGSOC and its unique potential role in chemotherapy-resistant disease.
引用
收藏
页数:35
相关论文
共 252 条
[1]   Inhibition of the JAK2/STAT3 pathway in ovarian cancer results in the loss of cancer stem cell-like characteristics and a reduced tumor burden [J].
Abubaker, Khalid ;
Luwor, Rodney B. ;
Zhu, Hongjian ;
McNally, Orla ;
Quinn, Michael A. ;
Burns, Christopher J. ;
Thompson, Erik W. ;
Findlay, Jock K. ;
Ahmed, Nuzhat .
BMC CANCER, 2014, 14
[2]   Targeted disruption of the JAK2/STAT3 pathway in combination with systemic administration of paclitaxel inhibits the priming of ovarian cancer stem cells leading to a reduced tumor burden [J].
Abubaker, Khalid ;
Luwor, Rodney B. ;
Escalona, Ruth ;
McNally, Orla ;
Quinn, Michael A. ;
Thompson, Erik W. ;
Findlay, Jock K. ;
Ahmed, Nuzhat .
FRONTIERS IN ONCOLOGY, 2014, 4
[3]   Short-term single treatment of chemotherapy results in the enrichment of ovarian cancer stem cell-like cells leading to an increased tumor burden [J].
Abubaker, Khalid ;
Latifi, Ardian ;
Luwor, Rod ;
Nazaretian, Simon ;
Zhu, Hongjian ;
Quinn, Michael A. ;
Thompson, Erik W. ;
Findlay, Jock K. ;
Ahmed, Nuzhat .
MOLECULAR CANCER, 2013, 12
[4]   Epithelial Mesenchymal Transition and Cancer Stem Cell-Like Phenotypes Facilitate Chemoresistance in Recurrent Ovarian Cancer [J].
Ahmed, N. ;
Abubaker, K. ;
Findlay, J. ;
Quinn, M. .
CURRENT CANCER DRUG TARGETS, 2010, 10 (03) :268-278
[5]   Epithelial-mesenchymal interconversions in normal ovarian surface epithelium and ovarian carcinomas: An exception to the norm [J].
Ahmed, Nuzhat ;
Thompson, Erik W. ;
Quinn, Michael A. .
JOURNAL OF CELLULAR PHYSIOLOGY, 2007, 213 (03) :581-588
[6]   Tumour microenvironment and metabolic plasticity in cancer and cancer stem cells: Perspectives on metabolic and immune regulatory signatures in chemoresistant ovarian cancer stem cells [J].
Ahmed, Nuzhat ;
Escalona, Ruth ;
Leung, Dilys ;
Chan, Emily ;
Kannourakis, George .
SEMINARS IN CANCER BIOLOGY, 2018, 53 :265-281
[7]   Unique proteome signature of post-chemotherapy ovarian cancer ascites-derived tumor cells [J].
Ahmed, Nuzhat ;
Greening, David ;
Samardzija, Chantel ;
Escalona, Ruth M. ;
Chen, Maoshan ;
Findlay, Jock K. ;
Kannourakis, George .
SCIENTIFIC REPORTS, 2016, 6
[8]   Ovarian cancer stem cells: Molecular concepts and relevance as therapeutic targets [J].
Ahmed, Nuzhat ;
Abubaker, Khalid ;
Findlay, Jock K. .
MOLECULAR ASPECTS OF MEDICINE, 2014, 39 :110-125
[9]   Getting to know ovarian cancer ascites: opportunities for targeted therapy-based translational research [J].
Ahmed, Nuzhat ;
Stenvers, Kaye L. .
FRONTIERS IN ONCOLOGY, 2013, 3
[10]   Cancerous ovarian stem cells: Obscure targets for therapy but relevant to chemoresistance [J].
Ahmed, Nuzhat ;
Abubaker, Khalid ;
Findlay, Jock ;
Quinn, Michael .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2013, 114 (01) :21-34