000 -LEADER |
fixed length control field |
a |
003 - CONTROL NUMBER IDENTIFIER |
control field |
OSt |
005 - DATE AND TIME OF LATEST TRANSACTION |
control field |
20190314102615.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
fixed length control field |
181213b xxu||||| |||| 00| 0 eng d |
040 ## - CATALOGING SOURCE |
Original cataloging agency |
AIKTC-KRRC |
Transcribing agency |
AIKTC-KRRC |
100 ## - MAIN ENTRY--PERSONAL NAME |
9 (RLIN) |
7029 |
Author |
Kawade, V. S. |
245 ## - TITLE STATEMENT |
Title |
Therapeutic Potential of PI3K/Akt/mTOR Signalling Pathway: Effective Combination Therapy for Cancer |
250 ## - EDITION STATEMENT |
Volume, Issue number |
Vol. 80 (04) July-August |
260 ## - PUBLICATION, DISTRIBUTION, ETC. |
Place of publication, distribution, etc. |
Mumbai |
Year |
2018 |
Name of publisher, distributor, etc. |
Indian Journal of Pharmaceutical Science |
300 ## - PHYSICAL DESCRIPTION |
Pagination |
702-708 |
520 ## - SUMMARY, ETC. |
Summary, etc. |
Cell signalling mechanism plays a vital role in cell functioning. Imbalance and disregulation between these signals, such as phosphatidylinositol-3-kinase/protein kinase B/mammalian target of rapamycin signalling pathway; may lead to uncontrolled cell proliferation. Generation of drug resistance is the hurdle in current cancer treatment. Designing an effective combination therapy for inhibition of two or more proteins of a given pathway might help to overcome the drug resistance and side effect related issues in cancer treatment. In this regard, application of computational tools firstly to predict newer combinations against phosphatidylinositol-3-kinase, protein kinase b and mammalian target of rapamycin involved in a single pathway have been proposed. The results obtained using the computational tools were shortlisted based on Glide score and binding interactions of the drugs to the receptors of the pathway. One of the predicted combinations was further subjected to biological evaluation using the Western blot assay. The experimental results revealed synergistic effects that supported the predictions. The study also provided insights for the application and development of computational tools to predict newer combinations in a given network pharmacology. |
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM |
9 (RLIN) |
4639 |
Topical term or geographic name entry element |
PHARMACEUTICS |
700 ## - ADDED ENTRY--PERSONAL NAME |
9 (RLIN) |
7030 |
Co-Author |
Satpute, P. S. |
700 ## - ADDED ENTRY--PERSONAL NAME |
9 (RLIN) |
7031 |
Co-Author |
Dhulap, S. A. |
773 0# - HOST ITEM ENTRY |
Title |
Indian journal of pharmaceutical sciences |
Place, publisher, and date of publication |
New Delhi Indian Pharmaceutical Association |
International Standard Serial Number |
0250-474X |
856 ## - ELECTRONIC LOCATION AND ACCESS |
Link text |
Click here |
URL |
http://www.ijpsonline.com/articles/therapeutic-potential-of-pi3kaktmtor-signalling-pathway-effective-combination-therapy-for-cancer-3518.html |
942 ## - ADDED ENTRY ELEMENTS (KOHA) |
Source of classification or shelving scheme |
|
Koha item type |
Articles Abstract Database |