P173 Plasma and tumour tissue TP53-gene expression in patients with high grade serous advanced ovarian cancer

Author(s):  
J Martinez-Garcia ◽  
P Sanchez Henarejos ◽  
MD Jimenez Lucas ◽  
A Puertes Boix ◽  
A Anton Garcia ◽  
...  
2020 ◽  
Vol 31 (9) ◽  
pp. 1240-1250 ◽  
Author(s):  
J. Millstein ◽  
T. Budden ◽  
E.L. Goode ◽  
M.S. Anglesio ◽  
A. Talhouk ◽  
...  

2020 ◽  
Author(s):  
Shahan Mamoor

Ovarian cancer is the most lethal gynecologic cancer (1). We sought to identify genes associated with high-grade serous ovarian cancer (HGSC) by comparing global gene expression profiles of normal ovary with that of primary tumors from women diagnosed with HGSC using published microarray data (2, 3). We identified the forkhead box L2, (FOXL2) (4) as among the genes whose expression was most different in HGSC ovarian tumors. FOXL2 expression was significantly lower in ovarian tumors relative to normal ovary. FOXL2 has established roles in ovarian development (4, 5), and the FOXL2 gene is mutated in granulosa-cell tumors of the ovary (6). These data indicate FOXL2 might also be perturbed, at the level of gene expression, in high-grade serous ovarian cancers.


2021 ◽  
Author(s):  
Olivia Le Saux ◽  
Hélène Vanacker ◽  
Fatma Guermazi ◽  
Mélodie Carbonnaux ◽  
Clémence Roméo ◽  
...  

Homologous recombination deficiency and VEGF expression are key pathways in high-grade ovarian cancer. Recently, three randomized practice changing trials were published: the PAOLA-1, PRIMA and VELIA trials. The use of PARP inhibitors (PARPi) following chemotherapy has become standard of care in first line. Combination of PARPi with anti-angiogenic agents has demonstrated synergistic activity in preclinical study. This review summarizes the body of evidence supporting the efficacy and safety of the combination of PARPi and anti-angiogenic drugs in first-line homologous recombination deficiency high-grade ovarian cancer leading to US FDA and EMA approvals. This double maintenance is supported by: a large benefit with bevacizumab + olaparib compared with olaparib alone, a rationale for additive effect, and a good safety and cost-effective profile.


2016 ◽  
Vol 141 (1) ◽  
pp. 95-100 ◽  
Author(s):  
Boris Winterhoff ◽  
Habib Hamidi ◽  
Chen Wang ◽  
Kimberly R. Kalli ◽  
Brooke L. Fridley ◽  
...  

Oncogene ◽  
2004 ◽  
Vol 23 (49) ◽  
pp. 8171-8183 ◽  
Author(s):  
Loris De Cecco ◽  
Luigi Marchionni ◽  
Manuela Gariboldi ◽  
James F Reid ◽  
M Stefania Lagonigro ◽  
...  

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