000 -LEADER |
fixed length control field |
a |
003 - CONTROL NUMBER IDENTIFIER |
control field |
OSt |
005 - DATE AND TIME OF LATEST TRANSACTION |
control field |
20211124140404.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
fixed length control field |
211124b xxu||||| |||| 00| 0 eng d |
040 ## - CATALOGING SOURCE |
Original cataloging agency |
AIKTC-KRRC |
Transcribing agency |
AIKTC-KRRC |
100 ## - MAIN ENTRY--PERSONAL NAME |
9 (RLIN) |
14807 |
Author |
Mukherjee, Souvik |
245 ## - TITLE STATEMENT |
Title |
Cucurbita pepo and Cucurbitacin in the Management of Anti-proliferation by JAK/STAT Pathway |
250 ## - EDITION STATEMENT |
Volume, Issue number |
Vol.55(1), Jan-Mar |
260 ## - PUBLICATION, DISTRIBUTION, ETC. |
Place of publication, distribution, etc. |
Banaglore |
Name of publisher, distributor, etc. |
Association of Pharmaceutical Teachers of India (APTI) |
Year |
2021 |
300 ## - PHYSICAL DESCRIPTION |
Pagination |
1-10p. |
520 ## - SUMMARY, ETC. |
Summary, etc. |
Pumpkin (Cucurbita pepo) is capaciously recycled similar to food and in folk medicine throughout the world. It accords to genus Cucurbita (CCT) under family Cucurbitaceae. There are a plenty of important medicinal phyto-constituents belonging to cucurbitoside like triterpenoids, CART and CCT glycosides. A survey of the literature demonstrates that C. pepo, has the capacity to improve prostatic hyperplasia, urinary dysfunction and cytotoxic properties. Many pharmacological revisions have established its role in hepatoprotection, inhibition of Prst gland cancer (CNCR), anti (Ant) oxidant effects, inhibition of LuG, BRst and triple-negative BRst CNCR by blocking JAK/STAT signaling (Sgls) pathway (Ptw). It has also Ant microbial, Ant -inflammatory, Ant -diabetic and Ant ulcer activities by supporting its traditional claims. Establishment of C. pepo and cucurbitacin (CCBT) in the management of Ant -proliferation by JAK/STAT Ptw. Data towards writing this review are generated through exploration of different websites like MEDLINE (PubMed), Google Scholar, Science Direct, Scopus, Cochrane, SID and Magiran databases. We have selected 2016- 2018 duration for the same purpose. We have found 88 papers related to this topic. CCBT is found to arrest unlimited cell (CEL) division and respective apoptosis (Appt) in vitro and in vivo CNCR models. A plenty of molecular design targeting CCBT have been invented, such as fibrous-actin, Sgls transducer and activator of transcription (STAT), cyclooxygenase-2, etc. This review is minded at CCBT from C. pepo which dwindle the proliferation of human CNCR CEL through the JAK/STAT Ptw. |
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) |
14808 |
Co-Author |
Pal, Dilipkumar |
773 0# - HOST ITEM ENTRY |
Place, publisher, and date of publication |
Bengluru Association of Pharmaceutical Teachers of India (APTI) |
International Standard Serial Number |
0019-5464 |
Title |
Indian journal of pharmaceutical education and research |
856 ## - ELECTRONIC LOCATION AND ACCESS |
URL |
https://www.ijper.org/sites/default/files/IndJPhaEdRes_55_1_1_1.pdf |
Link text |
Click here |
942 ## - ADDED ENTRY ELEMENTS (KOHA) |
Source of classification or shelving scheme |
|
Koha item type |
Articles Abstract Database |