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Officer-in-Charge: Dr. Sorab Dalal

The Electron Microscope Facility at ACTREC is equipped with JEM 1400 PLUS, a Transmission electron microscope (JEOL, Japan) functioning at 120kV with magnification up to 12,00,000 X and 0.2nm resolution. The facility provides services for research and analysis of biological samples, nanoparticles and other applications.

Electron Microscopy ATLAS

Current Applications
  • The facility carries out sample preparation for routine electron microscopy, including resin block making (solid tissues, monolayer cell cultures, and cell suspensions) followed by ultrathin sectioning using Leica UC-7 ultramicrotome, contrasting, and acquisition.
  • The facility also carries out negative staining for small particles (<100nm) like bacteriophages, exosomes, nanoparticles, proteins and DNA.
  • The facility provides acquisition of immunogold labelled macromolecules to detect specific localization.
  • The facility provides elemental detection by Bruker EDS system

The major areas of electron microscopy analysis are,

  • Ultrastructure study of cell and tissue,
  • Studying the details at organelle level like mitochondrial changes, ER - mitochondrial interactions, mitochondrial cristae, cell membrane, nuclear architecture, golgi complexes etc.,
  • To check events of autophagy, apoptosis or necroptosis,
  • Characterization of exosomes, bacteriophages and nanoparticles,
  • Uptake and effect of nanoparticles / drugs / radiation on cells or tissue,
  • EDS analysis of nanoparticles
Sample Submission

Please write to the facility regarding your requirement for electron microscopy. The facility will provide the details as per the analysis requirement. The users are requested to discuss over email regarding their study and sample submission. The samples need to be submitted along with a duly filled requisition form. The requisition form will be provided by the facility on request.

Charges
ACTREC & DAEOther than ACTREC institutionsCorporate
Routine EM1000500010000
Routine EM + Immunogold labeling1500600012000
Negative staining80040008000

18% GST to be included in addition to the following charges.

Mode of Payment

The charges should be paid against the quotation or invoice to the following account. The epayment details will be provided by the facility on request. The transaction details should be sent by email to the facility. The acquisition will be carried out after the receipt of the payment is confirmed.

Contact

Facility-in-charge: Siddhi A. Redkar
Technical Officer ‘D’
Electron Microscope Facility
(Khanolkar Shodhika - 68)
ACTREC, TMC
Plot No.1 & 2, Sector 22
Kharghar, Navi Mumbai - 410 210.
022-27405000 / 022-68735000
Extension : 5545
Email : tem.facility@actrec.gov.in

EM Staff: Ms. Arpana Kadam, Scientific Assistant ‘C’
Mr. Shridhar Nadkar, Technician ‘F’

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Publications

2025

  1. Nazia Chaudhary et.al. Patient-derived Organoids and Xenografts Uncover Therapeutic Vulnerabilities in Colorectal Signet Ring Cell Carcinomas. Clin Cancer Res. 2025 Jan 29
  2. Nazia Choudhary et. al. Inhibiting de novo lipogenesis identifies a therapeutic vulnerability in therapy-resistant colorectal cancer. Redox Biology. Feb. 2025
  3. Narasimha Anaganti, Aman Kumar Ujaoney, Biochemical characterization and functional insights into DNA substrate-specific activities of a unique radiation-inducible DR1143 protein from Deinococcus radiodurans, International Journal of Biological Macromolecules 310 (April 2025) 143214
  4. Roma Dohara, Dibyendu Bhattacharyya (2025). Intra-Golgi Golgin PpSgm1 and GRIP domain Golgin PpImh1 synergistically mediate Golgi cisternal stacking. Journal of Cell Science. PMID: 263612. April 2025
  5. Priyanka Joshi, Sanjeev K. Waghmare, et. al., Establishment and characterization of patient derived tongue squamous cell carcinoma cell lines. Human Cell (2025) 38:102
  6. Darshan Mehta, Sanjeev K Waghmare, et.al, Establishment and molecular characterization of the novel cutaneous squamous cell carcinoma cell line from advanced stage Indian patient. Human Cell (May 2025) 38:108
  7. Monika A. Jaiswal, Sorab N. Dalal, et.al, 14-3-3ε inhibits premature centriole disengagement by inhibiting the activity of Plk1 and Separase. Journal of Cell Science (2025) June 2025
  8. Chetna, De Lab, Nanoscale

2024

  1. Megha Garg et.al., Implications of chronic moderate protein-deficiency malnutrition on doxorubicin pharmacokinetics and cardiotoxicity in early post-weaning stage, Life Sciences 350 (2024) 122765
  2. Vandan Nagar et.al. Characterization and Genome Analyses of the Novel Phages P2 and vB_AhydM-H1 Targeting Aeromonas hydrophila, PHAGE,
  3. Madhura Ketkar et al, Inhibition of PERK mediated UPR acts as a switch for reversal of residual senescence and as senolytic therapy in glioblastoma, Neuro-oncology, doi/10.1093/neuonc/noae134/7716143, 22 July 2024
  4. Pratham Phadte, et.al. Autophagy-mediated ID1 turnover dictates chemo-resistant fate in ovarian cancer stem cells. J Exp Clin Cancer Res (2024) 43:222
  5. Amol Lonare, Sorab N Dalal, 14-3-3σ restricts YY1 to the cytoplasm, promoting therapy resistance, and tumor progression in colorectal cancer, Int J Cancer, 2024 Sep 6
  6. Radha G., Manu Lopus et.al., Biochemical and in silico analysis of the binding mode of erastin with tubulin. Journal of biomolecular structure and dynamics
  7. Kimaya Meher, Manu Lopus, et.al., Induction of autophagy-dependent and caspase and microtubule-acetylation-independent cell death by phytochemical-stabilized gold nanopolygons in colorectal adenocarcinoma cells. The Royal Society of Chemistry, Nanoscale,2024,16,7976–7987

2023

  1. Shreosi Chatterjee, Abira Ganguly, Dibyendu Bhattacharyya. Reprogramming nucleolar size by genetic perturbation of the extranuclear Rab GTPases Ypt6 and Ypt32. FEBS Letters 2023, 598(2024) 283–301
  2. Aman Kumar Ujaoney, Narasimha Anaganti, Mahesh Kumar Padwal, Bhakti Basu Deinococcus lineage and Rad52 family-related protein DR0041 is involved in DNA protection and compaction. International Journal of Biological Macromolecules 125885
  3. Sushant S Navarange 1 2, Sanjay M Bane 1, Darshan Mehta 1 2, Sanket Shah 3 2, Sanjay Gupta 3 2, Sanjeev K Waghmare 4Epithelial-to-mesenchymal transition status correlated with ultrastructural features, and TP53 mutation in patient-derived oral cancer cell lines. Mol Biol Rep. 2023 Oct: 50(10):8469-8481
  4. Neha Mishra et.al. Structural implications of amyloidogenic rare variants Ser282Leu and Gln356Arg identified in h-BRCA1. Proteins. 2023;–14
  5. Suchita Dubey, Neha Mishra, Nabajyoti Goswami, M. Quadir Siddiqui, Ashok K. Varma, Multimodal approach to characterize the tetrameric form of human PML-RBCC domain and ATO-mediated conformational changes. International Journal of Biological Macromolecules 223 (2022) 468–478.
  6. Sukanya Rauniyar, Kshama Pansare, Asmita Sharda, Saurav Raj Singh, Panchali Saha, Murali Krishna Chilakapati, and Sanjay Gupta. Raman Spectroscopy Revealed Cell Passage-Dependent Distinct Biochemical Alterations in Radiation-Resistant Breast Cancer Cells. ACS Omega 2023, 8, 5522−5532.

2022

  1. Nazia Chaudhary, et. al. Plakophilin3 loss leads to an increase in autophagy and radio-resistance. Biochemical and Biophysical Research Communications. Volume 620, 10 September 2022, Pages 1-7
  2. Pallavi Shukla, Prerana Dange, et.al. ARID2 suppression promotes tumor progression and upregulates cytokeratin 8, 18 and β-4 integrin expression in TP53-mutated tobacco-related oral cancer and has prognostic implications. Cancer Gene Therapy (2022)
  3. Dongre HN, Mahadik S, Ahire C, Rane P, Sharma S, Lukmani F, Patil A, Chaukar D, Gupta S, Sawant SS (2022). Diagnostic and prognostic role of protein and ultrastructural alterations at cell-extracellular matrix junctions in neoplastic progression of human oral malignancy. Ultrastructural Pathology.

2021

  1. Kakoli Bose, Ajay Wagh, et.al., Loss of GSK-3β mediated phosphorylation in HtrA2 contributes to uncontrolled cell death with Parkinsonian phenotype. International Journal of Biological Macromolecules 180 (2021) 97–111.
  2. Aniketh Bishnu, et.al., Molecular imaging of the kinetics of hyperactivated ERK1/2-mediated autophagy during acquirement of chemoresistance. Cell Death and Disease (2021) 12:161.
  3. Rajendra J, Ghorai A, Dutt S. Heliyon. 2021 Nov 12;7(11):e08371. 14-3-3ζ negatively regulates mitochondrial biogenesis in GBM residual cells.
  4. Prasad Sulkshane, et.al., Elevated USP9X drives early-to-late-stage oral tumorigenesis via stabilisation of anti-apoptotic MCL-1 protein and impacts outcome in oral cancers. British Journal of Cancer
  5. Sheikh Burhan Ud Din Farooqee, et.al. PSMD9 ribosomal protein network maintains nucleolar architecture and WT p53 levels. Biochemical and Biophysical Research Communications 563 (2021) 105-112.

2020

  1. Sudeshna Roy Chowdhury, et.al., ER arrival sites associate with ER exit sites to create bidirectional transport portals. J. Cell Biol. 2020 Vol. 219 No.4.
  2. Asmita Sharda, et.al., Elevated HDAC activity and altered histone phospho-acetylation confer acquired radioresistant phenotype to breast cancer cells. Clinical Epigenetics (2020) 12:4
  3. Ekjot Kaur, et.al., Inhibition of SETMAR–H3K36me2–NHEJ repair axis in residual disease cells prevents glioblastoma recurrence.Neuro-Oncology 22(12), 1785–1796, 2020
  4. Salunkhe S, et al., Biochim Biophys Acta Bioenerg. 2020 Dec 1;1861(12):148300. Metabolic rewiring in drug resistant cells exhibit higher OXPHOS and fatty acids as preferred major source to cellular energetics.
  5. Devanshi Khare, et.al., Genomic and functional insights into the adaptation and survival of Chryseobacterium sp. strain PMSZPI in uranium enriched environment. Ecotoxicology and Environmental Safety 191 (2020) 110217.

2019

  1. Bhawik Kumar Jain, et.al., The golgin PpImh1 mediates reversible cisternal stacking in the Golgi of the budding yeast Pichia pastoris. Journal of Cell Science (2019) 132, jcs230672
  2. Kshama Pansare, et.al., Establishment and genomic characterization of gingivobuccal carcinoma cell lines with smokeless tobacco associated genetic alterations and oncogenic PIK3CA mutation. Scientific Reports

2018

  1. Salunkhe S et al., Int J Cancer. 2018 May 15;142(10):2175-2185. Inhibition of novel GCN5-ATM axis restricts the onset of acquired drug resistance in leukemia.
  2. S Sawant, et.al., Alterations in desmosomal adhesion at protein and ultrastructure levels during the sequential progressive grades of human oral tumorigenesis. Eur J Oral Sci 2018; 126: 251–262. DOI: 10.1111/eos.12426.
  3. Nilesh Kolhe, et.al., Responses exhibited by various microbial groups relevant to uranium exposure. Biotechnology Advances 36 (2018) 1828–1846.
  4. Pallavi Chandwadkar, et.al., Uranium biomineralization induced by a metal tolerant Serratia strain under acid, alkaline and irradiated conditions. Metallomics, 2018,10, 1078.
  5. Bhawik Kumar Jain, et.al., Identification and characterization of GRIP domain Golgin a. PpImh1 from Pichia pastoris. Yeast. 2018;35:499–506
  6. Manjoor Ali, et.al., Thorium Decorporation Efficacy of Rationally-Selected Biocompatible Compounds with Relevance to Human Application. Journal of Hazardous Materials 2018.
  7. Saurabh Kirolikar, Indraneel Mittra, et al, Prevention of radiation-induced bystander effects by agents that inactivate cell-free chromatin released from irradiated dying cells. Cell Death and Disease (2018) 9:1142.

2017

  1. SS Sawant et al., A nomogram for predicting the risk of neck node metastasis in pathologically node-negative oral cavity carcinoma. Oral Diseases.
  2. Mansa Gurjar et al., Plakophilin3 increases desmosome assembly, size and stability by increasing expression of desmocollin2. Biochemical and Biophysical Research Communications (2017) 2017, 495(1):768-774.
  3. Chauhan DS, De A et al., 2017. NIR light triggered shrinkable thermoresponsive PNVCL nanoshells for cancer theranostics. RSC Advances, 7(70), 44026–34.
  4. Shanavas A, De A et al., 2017. Glycol chitosan assisted in situ reduction of gold on polymeric template for anti-cancer theranostics. International Journal of Biological Macromolecules. [Published 22-11-2017].
  5. Sonali S Vishal , Sarika Tilwani, Sorab N Dalal, Plakoglobin localization to the cell border restores desmosome function in cells lacking 14-3-3γ. December 2017. Biochemical and Biophysical Research Communications 495(2).

2016

  1. Dmello C, et al., Vimentin-mediated regulation of cell motility through modulation of beta4 integrin protein levels in oral tumor derived cells. Int. J. Biochem Cell Biol. 2016 Jan;70:161-172. Epub 2015 Nov.29.
  2. Sulkshane P, Teni T. BH3 mimetic Obatoclax (GX15-070) mediates mitochondrial stress predominantly via MCL-1 inhibition and induces autophagy-dependent necroptosis in human oral cancer cells. Oncotarget. Aug 5;8(36):60060-60079, 2016.
  3. S Sawant, et al., (2016) Establishment of 3D Co-Culture Models from Different Stages of Human Tongue Tumorigenesis: Utility in Understanding Neoplastic Progression. PLoS ONE 11(8): e0160615.
  4. Mukhopadhyay, A., Sehgal, L., Bose, A., Gulvady, A., Senapati, P., Thorat, R., Basu, S., Bhatt, K., Hosing, A. S., Balyan, R., Borde, L., Kundu, T. K., and Dalal, S. N. 2016 14-3-3γ prevents centrosome amplification and neoplastic progression. Scientific Reports 6, Article number: 26580 (2016)

    2015

  1. Aravind Kumar Rengan, et al., In Vivo Analysis of Biodegradable Liposome Gold Nanoparticles as Efficient Agents for Photothermal Therapy of Cancer. Nano Lett. 2015, 15, 842−848.

Dr. Pradnya Kowtal
Officer-in-Charge: Dr. Pradnya Kowtal

The DNA sequencing facility has two automated DNA sequencers: an eight capillary Genetic Analyzer 3500 and a 48 capillary Genetic Analyzer 3730 from Applied Biosystems/ Thermofisher, both of which are used for DNA sequencing and fragment analysis. The average turnaround time to give out data is one working day after receiving samples. During the year 2017, the facility carried out a total of 25,459 reactions of which 13,718 were for sequencing and 11,741 were for fragment analysis. The facility also provided demonstration of Sanger sequencing to students and other visitors.

Dr. Dibyendu Bhattacharyya
Officer-in-Charge: Dr. Dibyendu Bhattacharyya

The ACTREC Digital Imaging facility (ADIF) is a state of the art imaging facility housing several advanced imaging platforms. At present, the facility boasts of the following high end instrumentation:

  • LSM510 confocal microscope
  • Multiphoton confocal LSM780 microscope
  • 3i Mariana spinning disk confocal microscope
  • Leica SP8 confocal microscope with STED super resolution system
  • Leica DMI600B microscope - from Bhattacharyya lab
  • Axio Imager Z1
  • Axiovert 200M

The facility provides microscopic acquisition and analysis services for wide-field and confocal platforms listed above, to the ACTREC faculty and students, and also to outsider users.

CIR
Officer-in-Charge: Mr. Uday Dandekar

The Common Instrument Room (CIR) Department serves as a centralised facility for advanced scientific instrumentation and analytical services, designed to support multidisciplinary research in cancer biology. The department provides access to state-of-the-art equipment for characterization, analysis, and testing, enabling students and research scholars to carry out high-quality experimental work efficiently.

The department aims to promote a culture of shared resources and optimal utilization of instruments by offering sophisticated instruments to in-house departments or external institutions. By integrating cutting-edge technology with expert technical support, the facility enhances research capabilities across diverse labs.

In addition to routine analytical services, it facilitates hands-on training to help users gain technical expertise and ensure the optimal use of resources. The department operates on a transparent, user-friendly booking system to maximize accessibility and efficiency.

All major equipment installed in the department have been covered under an annual maintenance contract in order to provide safe, sustainable, efficient and reliable facilities. The department has a dedicated team of technical experts, who provide necessary technical support to all the equipment installed at other research labs and facilities of the CRI to maintain the equipment in working condition and to reduce downtime of the equipment.

Overall, the Common Instrument Room Department plays a vital role in fostering scientific excellence through the effective utilization of shared research infrastructure.

Common Instrument Room
Management

Committee Members -

Student Members:
Ms. Priti Shenoy
Mr. Jinesh Maniar

Facility In-charge: Ms. Snehal Valvi
Email: snehal.valvi[at]actrec[dot]gov[dot]in

Facility Staff: Mr. Amandeep Jast
Email: jastaman[dot]actrec[at]gmail[dot]com

Contact Us

Molecular Imaging Facility
AH-105 and 107, First Floor, Laboratory Animal Facility, ACTREC, TMC
Plot No.1 & 2, Sector 22
Kharghar, Navi Mumbai - 410 210.
Contact: 022-27405000 / 022-68735000 and ask for extension 5682
Email: mifacility[at]actrec[dot]gov[dot]in

Dr. Abhijit De
Officer-in-Charge: Dr. Abhijit De

Considering the growing importance of detecting cancer in a whole-body context of preclinical model organisms that the researchers use in experimental settings, the Molecular Imaging Facility (MIF) was envisioned by Dr. Abhijit De. The MIF facility started its operation in 2013, offering advanced imaging capacity for both live cell population and preclinical in vivo imaging services to researchers. This core facility supports imaging based on three forms of photonic signatures, i.e. Bioluminescence, Cerenkov luminescence and Near InfraRed Fluorescent (NIRF), providing valuable molecular and functional information from whole body context. Current equipment provide ability to scan live cells and small animals to support longitudinal monitoring of disease progression, tracking therapy response and tracking biodistribution of labelled cells and materials. Fast scanning process allows rapid generation of high-quality imaging data for visualization and quantitative analysis. This facility has established track record of supporting imaging work for in-house researchers as well as external research collaborations with institutions and industries.

Facility Equipment and Imaging Support

The facility is currently equipped with three In Vivo Imaging Systems (IVIS) platforms along with supporting gadgets like gas anaesthesia and dedicated computing resources for image acquisition and analysis:

  1. IVIS Lumina II (PerkinElmer, USA)
  2. IVIS Spectrum (PerkinElmer, USA)
  3. IVIS Spectrum CT (Revvity, USA formerly PerkinElmer, USA)

IVIS Lumina II

  • Both live cell and live animal imaging in luminescence mode.
  • Allows scanning of upto 3 mice at a time.
  • Equipped with four standard fluorescence emission filters GFP, Cy5.5, DsRed and ICG.

IVIS Spectrum

  • Both live cell and live animal imaging in bioluminescence, Cerenkov luminescence and NIR fluorescence mode.
  • Allow upto 5 mice per scan in 2D planar mode and 1 mouse for 3D tomographic imaging mode
  • Wide range of filter set to support spectral unmixing (10 Excitation filters in the range of 430-745 nm, 35 nm bandwidth and 18 Emission filters covering 500-840 nm, 20 nm bandwidth). Spectral unmixing imaging capacity provides scope of using multiple probes emitting non-overlapping photonic signatures.

IVIS Spectrum CT

  • Both live cell and live animal imaging in bioluminescence, Cerenkov luminescence and NIR fluorescence mode.
  • Allow upto 5 mice in 2D planar scanning mode and upto 2 mouse for 3D scanning mode
  • This system provides full 3D tomographic imaging support with coregistered optical signals with precise anatomical (CT) images for volumetric reconstruction of molecular signals.
  • Wide range of filter set to support spectral unmixing (10 Excitation filters in the range of 430-745 nm, 35 nm bandwidth and 18 Emission filters covering 500-840 nm, 20 nm bandwidth). Spectral unmixing imaging capacity provides scope of using multiple probes emitting non-overlapping photonic signatures.
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Applications
  1. Non-invasive, real-time in vivo imaging allowing longitudinal monitoring of disease progression.
  2. Primarily used for oncology research applications using rodent models (Xenografts, Syngeneic Tumor Models, Orthotopic and Metastasis models); can be extended to other areas like inflammatory, infectious and neuronal disease models.
  3. Efficacy measurement of various forms of therapy interventions and biodistribution and uptake studies to understand material cellular distribution in whole animal context.
  4. Imaging stem cell graft differentiation, testing cell / medical implants in vivo using suitable phantom or model system.
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User Guidelines
  • Users are required to submit signed End User Form before starting new experiments. Email the End User at Form to - Email id mifacility[at]actrec[dot]gov[dot]in
  • An online booking software is created to book imaging slots. Users can book slots via URL http://10.100.36.253/FacilityEquipBooking by entering last 6 digits of their CC number and password.
  • Booking slots open a week before; no more than 2 consecutive time slots can be booked by any user.
  • External service users can contact MIF facility directly and discuss requirements.
Management

Committee Members -

Student Members:
Ms. Priti Shenoy
Mr. Jinesh Maniar

Facility In-charge: Ms. Snehal Valvi
Email: snehal.valvi[at]actrec[dot]gov[dot]in

Facility Staff: Mr. Amandeep Jast
Email: jastaman[dot]actrec[at]gmail[dot]com

Contact Us

Molecular Imaging Facility
AH-105 and 107, First Floor, Laboratory Animal Facility, ACTREC, TMC
Plot No.1 & 2, Sector 22
Kharghar, Navi Mumbai - 410 210.
Contact: 022-27405000 / 022-68735000 and ask for extension 5682
Email: mifacility[at]actrec[dot]gov[dot]in

Dr. Sanjay Gupta
Officer-in-Charge: Dr. Sanjay Gupta

The Common Facilities (CF) operates and maintains support services like X-ray developing machine, ultra-pure water purification system, radioactive handling room for 32P and 125I, bacterial culture hoods, ice making machines and cold room facility to different research groups. In addition, maintenance of all the autoclaves and ovens belonging to different research groups is handled by the CF technicians.

All the major equipment under common facility is covered under annual maintenance contract in order to provide safe, sustainable, efficient and reliable facilities.

Dr. Poonam Gera
Officer-in-Charge: Dr. Poonam Gera

The ACTREC Biorepository is the custodian of stored biological samples that can be shared, under a tightly regulated and strictly monitored mechanism, with researchers having approved projects that aim to study the biology of cancer, find biomarkers for a more refined molecular classification, or for targeted therapy. In all, tissue samples from 630 cases were accrued in the Biorepository during 2017. As always the majority were head and neck tumors, followed by breast tumors. Other tumor types included neurological, gastrointestinal, genitourinary, gynecological, etc.

This year, the collection of bio specimens was extended to the Breast OPD wherein core biopsies are now being cryo preserved for future research; this is in addition to collection from the OTs, Frozen room and Surgical Pathology. Cryopreserved tissue samples (470) were provided to eight Principal Investigators with approved projects under various protocols at the Tata Memorial Centre. In the International Cancer Genome Consortium (ICGC) project, gingivo buccal mucosa tumour and blood samples were collected from 30 patients accrued this year, and their extracted genomic DNA samples were sent to NIBMG, Kalyani for whole genome scan and sequence capture-based flow cell sequencing.

The Biorepository itself initiated a project on quality monitoring of in-house cryo preserved tissues. The OIC contributed her Pathology expertise involving the evaluation of Hematoxylin & Eosin as well as immunohistochemistry slides to eight ACTREC projects.

Dr. Ashok Varma
Officer-in-Charge: Dr. Ashok Varma

The Bioinformatics facility of ACTREC provides infrastructural and technical support to scientists, clinicians and research scholars of the Centre to fulfil the bioinformatics requirements of their on-going research projects. Scientists of the Centre also use the facility’s infrastructure to explore microarray, next generation sequence data analysis, database development, molecular modelling and data mining for their on-going projects.

This facility receives strong funding support from DBT and is established as a BTIS-net centre of this region. It is well equipped with one nVIDIA Tesla GPU workstation, 5 workstations, 1 webserver and seven PCs. The facility also focuses on database development such as Histome: the human infobase; this database is presently being updated. In the domain of gene expression studies, projects related to TGCA database mining and analysis are under progress. In silico molecular modelling, dynamics and protein-protein interactions have been performed using BARC’s supercomputing facility.

The facility hosted a national 28th BTISnet Coordinators Meeting on 3rd and 4th February 2017. The facility also organized its annual 2-day Workshop on ‘Basics of Bioinformatics’ targeting college teachers and research scholars of institutions in the Mumbai and neighboring areas on 2nd and 3rd March 2017. The facility staff also provided training to six trainees during the year, three for Bachelor’s/ Master’s dissertation and three for experience.

Dr K Nirmal Kumar
Officer-in-Charge: Dr K Nirmal Kumar

The Anti-Cancer Drug Screening Facility (ACDSF) at ACTREC supports the efforts of anti-cancer drug development in India, with in vitro and in vivo anti-cancer drug screening assays that have been developed in-house. ACDSF has 53 human tumor cell lines, 10 murine tumor models and 38 xenograft models for carrying out drug screening. During 2017, 1345 compounds were received from 161 clients including eight corporate R&D organizations from 13 states across India. In all, 1287 compounds were tested for their in vitro activity and 58 compounds were examined for MTD (n=14) and in vivo efficacy assays (n=44).

Two new xenografts namely KG-1 (leukemia) and HCC1954 (breast cancer) were developed during the report year. The facility has successfully completed XII-plan CSIR funded project ‘Affordable cancer therapeutics’ in collaboration with IICT, Hyderabad (2012-17). Of the second set of 300 compounds, 11 compounds were found to be active against four cancer cell lines (Hep-G2, HT-29, SCC-29B and PLC-Prf-5).

Temporary Suspension of Testing Services

Three of these compounds that were most active against oral cancer spheroids (CSC) were further tested for their in vivo efficacy against oral cancer xenograft AW13516. Only one of these (AKL-JA) was found to be strongly active against the AW13516 xenograft. Corroborative evidence was obtained through PET-CT imaging of tumor bearing animals and histopathology of tumor sections.

Contact Us

For sample submission and enquiry: Please write to the facility in charge for further information on service provided, sample submission and requisition form will be provided by the facility. Users are requested to discuss over email/telephone regarding the study and other information.

Contact:
Facility in charge: Dr K Nirmal Kumar,
Scientific Officer ‘D’
Anti-Cancer Drug Screening,
Room No. KS-324,
Advanced Centre for Treatment, Research & Education in Cancer (ACTREC),
Tata Memorial Centre,
Kharghar, Navi Mumbai - 410 210.
Email: acdsf@actrec.gov.in
Tel: 022-27405000 / 022-68735000
Ext: 5431

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