Stem cell markers: ABCG2 and MCM2 expression in retinoblastoma

被引:42
作者
Mohan, A.
Kandalam, M.
Ramkumar, H. L.
Gopal, L.
Krishnakumar, S.
机构
[1] Vis Res Fdn, Dept Ocular Pathol, Madras 600006, Tamil Nadu, India
[2] Northwestern Univ, Dept Sci Biol, Evanston, IL 60208 USA
[3] Vis Res Fdn, Vitreoretina Serv, Madras 600006, Tamil Nadu, India
关键词
D O I
10.1136/bjo.2005.089219
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Backgound/aim: The authors studied the expression of cancer stem cell surface marker, ABCG2, and neural stem cell marker, MCM2, in retinoblastoma and correlated clinicopathologically. Methods: Among 39 retinoblastomas, 18 tumours were not subjected to preoperative/postoperative chemotherapy, 15 tumours underwent postoperative chemotherapy, and six tumours had preoperative chemotherapy. There were 20 tumours with no invasion and 19 tumours with invasion of choroid/optic nerve. ABCG2 and MCM2 expression was studied by immunohistochemistry. Results: ABCG2 was positive in six of six and MCM2 was positive in five of six tumours that had recurred in the orbit or metastasised. ABCG2 was positive in 15/19 tumours with invasion. MCM2 was positive in 16/19 tumours with invasion. Invasive tumours showed higher expression of ABCG2 (p < 0.01) and MCM2 (p < 0.01) proteins. There was no correlation with differentiation and laterality of the tumours. Nonneoplastic retina was positive for ABCG2 and MCM2. Conclusion: ABCG2 and MCM2 were expressed more in invasive tumours. Further studies are needed to understand the significance of ABCG2 and MCM2 expression in retinoblastoma.
引用
收藏
页码:889 / 893
页数:5
相关论文
共 20 条
[1]  
Allen JD, 1999, CANCER RES, V59, P4237
[2]   Frequent expression of the multi-drug resistance-associated protein BCRP/MXR/ABCP/ABCG2 in human tumours detected by the BXP-21 monoclonal antibody in paraffin-embedded material [J].
Diestra, JE ;
Scheffer, GL ;
Català, I ;
Maleipaad, M ;
Schellens, JHM ;
Scheper, RJ ;
Germà-Lluch, JR ;
Izquierdo, MA .
JOURNAL OF PATHOLOGY, 2002, 198 (02) :213-219
[3]   Mcm2, Geminin, and Ki67 define proliferative state and are prognostic markers in renal cell carcinoma [J].
Dudderidge, TJ ;
Stoeber, K ;
Loddo, M ;
Atkinson, G ;
Fanshawe, T ;
Griffiths, DF ;
Williams, GH .
CLINICAL CANCER RESEARCH, 2005, 11 (07) :2510-2517
[4]   The search for the retinoblastoma cell of origin [J].
Dyer, MA ;
Bremner, R .
NATURE REVIEWS CANCER, 2005, 5 (02) :91-101
[5]   Recommendations for the reporting of tissues removed as part of the surgical treatment of common malignancies of the eye and its adnexa [J].
Folberg, R ;
Salomao, D ;
Grossniklaus, HE ;
Proia, AD ;
Rao, NA ;
Cameron, JD .
AMERICAN JOURNAL OF SURGICAL PATHOLOGY, 2003, 27 (07) :999-1004
[6]  
Freeman A, 1999, CLIN CANCER RES, V5, P2121
[7]   A new proliferation marker, minichromosome maintenance protein 2, is associated with tumor aggressiveness in esophageal squamous cell carcinoma [J].
Kato, H ;
Miyazaki, T ;
Fukai, Y ;
Nakajima, M ;
Sohda, M ;
Takita, J ;
Masuda, N ;
Fukuchi, M ;
Manda, R ;
Ojima, H ;
Tsukada, K ;
Asao, T ;
Kuwano, H .
JOURNAL OF SURGICAL ONCOLOGY, 2003, 84 (01) :24-30
[8]   The role of MCM proteins in the cell cycle control of genome duplication [J].
Kearsey, SE ;
Maiorano, D ;
Holmes, EC ;
Todorov, IT .
BIOESSAYS, 1996, 18 (03) :183-190
[9]   Multidrug resistant proteins: P-glycoprotein and lung resistance protein expression in retinoblastoma [J].
Krishnakumar, S ;
Mallikarjuna, K ;
Desai, N ;
Muthialu, A ;
Venkatesan, N ;
Sundaram, A ;
Khetan, V ;
Shanmugam, MP .
BRITISH JOURNAL OF OPHTHALMOLOGY, 2004, 88 (12) :1521-1526
[10]  
Litman T, 2000, J CELL SCI, V113, P2011