Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sanjay M. Bane"'
Autor:
Chella Krishna Vadivel, Subeer S. Manjumdar, Shweta Patel, Shruti Sinha, Rahul Thorat, Nirmalya Ganguli, Milind M. Vaidya, Sayli Jamghare, Hunain Alam, Richa Tiwari, Indrajit Sahu, Sanjay M. Bane
Publikováno v:
Cell Biology International. 45:1720-1732
Keratin 8/18, the predominant keratin pair of simple epithelia, is known to be aberrantly expressed in several squamous cell carcinomas (SCCs), where its expression is often correlated with increased invasion, neoplastic progression, and poor prognos
Autor:
Arvind Ingle, Rajiv P. Gude, Archana Upadhya, Manohar C. Dange, Rabindranath Mukhopadhyaya, Rajiv D. Kalraiya, Nithya Srinivasan, Shyam K. More, Sanjay M. Bane
Publikováno v:
Clinical & Experimental Metastasis. 31:661-673
Interactions between molecules on the surface of tumor cells and those on the target organ endothelium play an important role in their arrest in an organ. Galectin-3 on the lung endothelium and high affinity ligands poly-N-acetyllactosamine (polyLacN
Autor:
Shubhada V. Chiplunkar, Archana Upadhya, Rajiv D. Kalraiya, Shyam K. More, Sanjay M. Bane, Srikanth Budnar, Rahul Thorat, Nithya Srinivasan, Arvind Ingle
Publikováno v:
Biochemical and biophysical research communications. 460(2)
Poly-N-acetyl-lactosamine (polyLacNAc) on N-glycans facilitate lung specific metastasis of melanoma cells by serving as high affinity ligands for galectin-3, expressed in highest amounts in the lungs, on almost all its tissue compartments including o
Publikováno v:
Glycoconjugate journal. 26(4)
Galectin-3 on vascular endothelium has been shown to facilitate lung specific metastasis. Metastatic variants of B16 melanoma were chosen to identify specific ligands that mediate lung colonization via galectin-3. Flow cytometry showed that, galectin
Publikováno v:
Clinicalexperimental metastasis. 22(1)
Adhesive interactions between the molecules on cancer cells and the target organ are one of the key determinants of the organ specific metastasis. In this communication we show that b1,6 branched N-oligosaccharides which are expressed in a metastasis