Cancer is a major cause of morbidity and mortality world
over. In 1996, anticancer programme was initiated as the
national facility at the Institute with the objective
to develop anticancer therapeutics from natural sources
such as plants, fungi and bacteria. Later, semi-synthetic
and synthetic molecules were also included. We have state
of art facilities for in vitro cytotoxicity studies against
human cancer cell lines, in vivo murine tumor models for
in vivo anticancer studies and in vitro mechanistic studies
for carrying out the target based diverse studies for
the discovery of novel anti-cancer chemotherapeutics.
Interest is growing in the posttranslational modifications
that comprise mainly the evaluation of histone code and
their relationship to cancer development. This is because;
the perturbation of normal histone modifications has been
associated with undesirable cellular phenotypic changes
in cancer.
In addition, a small group is also involved in the search
for hepatoprotective agents from selected medicinal plants
for the development of safe, efficacious, chemically defined,
biologically standardized and economical herbal preparation/molecules.
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Discovery of anticancer therapeutics
form natural products. |
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Conducts and supports research, training,
and other programs with respect for cancer research.
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The group has competencies/expertise in the following
area
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In vitro cytotoxicity
against human cancer cell lines. |
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In vivo anticancer
activity against murine models such as Ehrlich Ascites
Carcinoma, Ehrlich Tumor (solid), Sarcoma-180 Ascites,
Sarcoma-180 (solid), Methyl cholanthere induced
ascites, L1210 Lymphoid leukemia, P388 Lymphocytic
leukemia. |
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Event based mechanistic
studies
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Detection of nuclei condensation
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Detection of apoptosis / necrosis
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Cell cycle analysis |
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ROS estimation |
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Nitric oxide estimation |
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Mitochondrial membrane potential
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Tunnel Assay for apoptosis |
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Intracellular Calcium measurement
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DNA fragmentation |
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Genotoxicity COMET Assay |
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Target based mechanistic
studies
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Apoptotic Signaling Cascades
TNF-R1, Fas, DR4, Bcl-2, Bcl-xL, Bax, Cyt
C, Bid, Nf-kB, IkB, Surviivn, HSP70, HSP-90,
STAT-3, Akt, PI-3, Telomerase, iNOS , DRP-1,
Smac/Diablo, AIF etc. |
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Determination of Caspases activity
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Topoisomerase I & II |
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| Sr. NO |
Name |
Sr. No. |
Name |
| 1. |
Ravinder Kaur |
2 |
Neelam Sharma |
| 3. |
Kuldeep Singh |
3 |
Jasbir Singh |
| 5. |
Santosh Baigra |
|
|
| 1. |
Ajay Kumar |
2 |
Satyam K Agrawal |
| 3. |
Madhunika Sharma |
4 |
Harish Chandra Pal |
| 5. |
Irum Sehar |
6 |
Gousia Chashoo |
| 7. |
Sheema Khan |
8 |
Arpita Saxena |
| 9. |
Zahoor Ahmad Wani |
10 |
Nidhi Sharma |
| 11. |
Yasrib Qurishi |
12 |
Tandeep Kaur |
| 13. |
Rabia Majeed |
14 |
Asif Khurshid Qazi |
| 15. |
Bilal Ahmad Rah |
16 |
Nitasha Suri |
Anticancer Drug Discovery
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Cell Culture Facilitiesc |
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In Vivo Facilities in Animal Isolators
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Cytometer with Cell Sorter |
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Confocal & Electron Microscope |
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Gel Documentation System |
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ELISA Reader |
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Multiplate Detection Reader (UV-visible,
Fluorescence, Illumnicence) |
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Robotic Liquid Handling System Aided
MTS |
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Electroblotter |
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PCR Machine( Thermocycler
) |
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Other Accessories [Deep Freezers (-20°C,-80°C);
Refrigerated Centrifuges; Protein, RNA & DNA Electrophoretic
Apparatus; Magnetic Stirrer; pH Meter; Water Bath;
High Precision Weighing Balance etc] |
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Plant extracts, microbial extracts, fungal extracts, semi-synthetic
molecules, synthetic molecules are being evaluated for
their in vitro cytotoxicity against human cancer cell
lines. The promising extracts are subjected to bio-assay
guided fractionation for isolation of active fraction(s)/molecule(s).
The active isolates / compounds are subjected to in vivo
anticancer activity using murine models to determine their
real potential. The isolates / compounds active in vivo
are further subjected to target / event based mechanistic
studies to determine their mode of action.
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| 1. |
SUPRA-INSTITUTIONAL PROJECT: Development
of novel target based anti- cancer therapeutics
(SIP-0027). |
| 2. |
CSIR NETWORK PROJECT: Discovery and
preclinical studies of new bioactive molecules (natural
& semi-synthetic) and traditional preparations.
(NWP-0037). |
| 3. |
CSIR NETWORK R & D PROJECT: Biological
and chemical transformation of plant compounds for
production of value added products of therapeutic/aroma
activity (NWP-0009). |
| 4. |
RC APPROVED PROJECT: Resourcing of
biomolecules from medicinal plants and microflora
including higher fungi (MLP-3008). DST funded project:
Evaluation of 2-chloroethylnitrosourea derivatives
of substituted naphthalimides as novel group of
anticancer agents. |
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