Carbon nanospheres mediated nuclear delivery of SMAR1 protein (DNA binding domain) controls breast tumor in mice model
被引:3
|
作者:
Bhagat, Prasad N.
论文数: 0引用数: 0
h-index: 0
机构:
Agharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, IndiaAgharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, India
Bhagat, Prasad N.
[1
]
Jadhav, Sachin H.
论文数: 0引用数: 0
h-index: 0
机构:
Agharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, IndiaAgharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, India
Jadhav, Sachin H.
[1
]
Chattopadhyay, Samit
论文数: 0引用数: 0
h-index: 0
机构:
Natl Ctr Cell Sci, SP Pune Univ Campus,Ganeshkhind Rd, Pune 411007, Maharashtra, India
Indian Inst Chem Biol, 4 Raja SC Mullick Rd, Kolkata 700032, IndiaAgharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, India
Chattopadhyay, Samit
[2
,3
]
Paknikar, Kishore M.
论文数: 0引用数: 0
h-index: 0
机构:
Agharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, IndiaAgharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, India
Paknikar, Kishore M.
[1
]
机构:
[1] Agharkar Res Inst, GG Agarkar Rd, Pune 411004, Maharashtra, India
[2] Natl Ctr Cell Sci, SP Pune Univ Campus,Ganeshkhind Rd, Pune 411007, Maharashtra, India
[3] Indian Inst Chem Biol, 4 Raja SC Mullick Rd, Kolkata 700032, India
Aim: To investigate anticancer activity of the DNA binding domain of SMAR1 (His 5) in vitro and in vivo. Materials & methods: His 5 was conjugated to hydrothermally synthesized carbon nanospheres (CNs). Anticancer activity of CNs-His 5 was evaluated in vitro and in vivo. Results: CNs-His 5 significantly reduced cyclin D1 levels in MDA-MB-231 cells. Tumor bearing Balb/c mice injected with CNs-His 5 showed approximately 62% tumor regression and significantly reduced (18)FDG uptake. Caspases assay and IHC staining confirmed tumor growth inhibition, which could be attributed to apoptotic, antiproliferative and antiangiogenic activities of His 5. Conclusion: DNA binding domain of the SMAR1 protein (His 5) has potent anticancer activity and its CNs mediated delivery could control breast tumor in mice model.