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1.
Mycologia ; 114(1): 157-174, 2022.
Article in English | MEDLINE | ID: mdl-34797203

ABSTRACT

Stem rot by Ganoderma is a disease of major concern for coconut farmers. Many species (G. applanatum, G. boninense, G. lucidum, G. zonatum) have been implicated as the causal agents of the disease. Despite its importance, systematics of the rot-associated Ganoderma remains uncertain and unresolved. Morphologically heterogeneous basidiomata of the putative pathogen(s) from infected palms in multiple disease sites were collected during an outbreak in the coastal state of India, Kerala. Morphological and molecular investigations revealed that these specimens were distinct from all the Ganoderma species so far identified and reported from coconut. Although with a close morphological resemblance to many Ganoderma species collected from palms, they exhibited unique genetics and geographic distribution patterns. We present a taxonomic reassessment of the species collected from infected coconut palms in India and also propose two new species, Ganoderma keralense and G. pseudoapplanatum. A taxonomic key to Ganoderma species on palms is given.


Subject(s)
Arecaceae , Ganoderma , Cocos , Ganoderma/genetics , India
2.
Indian J Orthop ; 55(4): 953-960, 2021 Aug.
Article in English | MEDLINE | ID: mdl-34194653

ABSTRACT

AIM: The objective of the study is to compare the accuracy of implant positioning and limb alignment achieved in robotic-arm assisted total knee arthroplasty(RATKA) and manual total knee arthroplasty(MTKA) to their respective preoperative plan. PATIENTS AND METHODS: This was a prospective observational study conducted in a tertiary care centre between August 2018 and January 2020. 143 consecutive RATKA(105 patients) and 151 consecutive MTKA(111 patients) performed by two experienced arthroplasty surgeons were included. Two independent observers evaluated the accuracy of implant positioning by measuring the radiological parameters according to the Knee-Society-Roentgenographic-Evaluation-System and limb alignment from postoperative weight-bearing scanogram. Outcomes were defined, based on the degree of deviation of measurements from the planned position and alignment, as excellent(0-1.99°), acceptable(2.00-2.99°) and outlier(≥ 3.00°). RESULTS: There were no systematic differences in the demographic and baseline characteristics between RATKA and MTKA. Statistically significant outcomes were observed favouring robotic group for postoperative mechanical axis (p < .001), coronal inclination of the femoral component (p < 0.001), coronal inclination of tibial component (p < 0.001), and sagittal inclination of tibial component (p < 0.001). There was no significant difference in the sagittal inclination of the femoral component (p = 0.566). The percentage of knees in the 'excellent' group were higher in RATKA compared to MTKA. There was absolutely no outlier in terms of limb alignment in the RATKA group versus 23.8% (p < 0.001) in the MTKA group. All the measurements showed high interobserver and intraobserver reliability. CONCLUSION: Robotic-arm assisted TKA executed the preoperative plan more accurately with respect to limb alignment and implant positioning compared to manual TKA, even when the surgeons were more experienced in the latter. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s43465-020-00324-y.

4.
J Nanosci Nanotechnol ; 20(12): 7710-7715, 2020 Dec 01.
Article in English | MEDLINE | ID: mdl-32711647

ABSTRACT

We synthesis different sizes of cadmium selenide quantum dots (CdSe QDs) and their linear and nonlinear optical properties. Size-controlled CdSe QDs are characterized by ultraviolet-visible absorption, photoluminescence, transmission electron microscope (TEM), and Z-scan techniques. Redshift was observed in the linear absorption and photoluminescence with an increase in the size of CdSe QDs. TEM images show the sizes of the QDs are 2.2 nm-4.9 nm. Bandgap tuning CdSe QDs of third-order nonlinear optical properties are investigated at 532 nm with an open aperture Z-scan technique using a picosecond laser. These CdSe QDs can be used as optical limiters.

5.
Lett Appl Microbiol ; 71(1): 108-116, 2020 Jul.
Article in English | MEDLINE | ID: mdl-31602688

ABSTRACT

The indiscriminate use of antimicrobials in aquaculture results in antibiotic selection pressure and proliferation of antimicrobial resistant (AMR) bacteria. Frequent assessment of antimicrobial resistance in aquaculture environment is inevitable so as to reduce the passage of clinically important AMR from aquatic to other environment. The present study analysed the antimicrobial resistance of pathogens associated with diseased koi carp and goldfish from an ornamental fish farm. Phenotypic and genotypic characterization of the recovered isolates from both fishes revealed significant pathogens in aquaculture such as Aeromonas, Edwardsiella tarda, Acinetobacter, Lactococcus, Citrobacter, Enterobacter and Comamonas. Shannon-Wiener diversity of koi isolates (2·359) was found to be higher than that of goldfish (1·864). Antibiotic susceptibility testing using disc diffusion with 47 antibiotics revealed significant resistance pattern of Acinetobacter, Comamonas, Klebsiella and Enterobacter from goldfish and Edwardsiella, Aeromonas, Lactococcus, Enterobacter and Acinetobacter from koi with higher multiple antibiotic resistance indexes (>0·3). The minimum inhibitory concentration of antibiotics for the major resistant isolates was found to be very high with >256 µg. All the isolates were susceptible to amoxicillin, kanamycin, cefepime, cefexime, cefotaxime, ceftazidime, doripenem, ciprofloxacin and norfloxacin, recommending their successful application in the farm. SIGNIFICANCE AND IMPACT OF THE STUDY: Antimicrobial resistance is a major threat faced in aquaculture industry. The current study provides baseline information regarding the antibiotic resistance patterns of diverse pathogens recovered from ornamental koi carp and goldfish. The higher MAR index of pathogens and greater MIC of antibiotics for the resistant isolates highlighted the intense use of antibiotics in aquaculture farm. The potential of the pathogens to exhibit resistance even towards the new generation antibiotics remind the need of prudent use of antibiotics and continuous monitoring and surveillance programmes.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacteria/genetics , Carps/microbiology , Fresh Water/microbiology , Goldfish/microbiology , Animals , Aquaculture , Bacteria/classification , Bacteria/drug effects , Bacteria/isolation & purification , Farms , Fishes/microbiology , Humans , Microbial Sensitivity Tests
6.
J Food Sci Technol ; 56(2): 713-723, 2019 Feb.
Article in English | MEDLINE | ID: mdl-30906029

ABSTRACT

Quality protein maize (QPM) is nutritionally improved maize which has twice the amount of lysine and tryptophan than normal maize. The present study evaluated the effect of different proteins namely egg white proteins (EWP), casein, whey protein isolate, soy protein isolate (SPI) on characteristics of gluten free QPM based muffins. QPM muffins without any added protein served as control and muffins prepared using wheat and EWP served as reference. Effect of addition of different proteins on pasting properties revealed that the thermal stability of QPM flour increased as indicated by decrease in breakdown viscosity. The effect of added proteins on QPM muffin-making properties was evaluated for rheology of batter and physicochemical, texture, color and sensory characteristics of muffins. Dynamic rheology showed that storage modulus (G') and loss modulus (G″) of batter with SPI was the highest while batter with EWP showed lowest value. QPM-EWP muffins were softer, chewy and springier and had more specific volume than control muffins and were comparable to reference muffins. Inclusion of all proteins increased L* values (lightness) and decreased a* (redness/greenness) and b* (yellow/blueness) values of QPM based muffins. Sensory analysis revealed that gluten free QPM muffin prepared from EWP were acceptable with a sensory score of 7.97 which was comparable to reference muffins (8.03).

7.
Oncotarget ; 8(64): 107374-107389, 2017 Dec 08.
Article in English | MEDLINE | ID: mdl-29296172

ABSTRACT

Nanoencapsulation has emerged as a novel strategy to enhance the pharmacokinetic and therapeutic potential of conventional drugs. Recent studies from our lab have established the efficacy of curcumin in sensitizing cervical cancer cells and breast cancer cells towards paclitaxel and 5-FU chemotherapy respectively. Factors that hinder the clinical use of curcumin as a sensitizer or therapeutic agent include its poor bioavailability and retention time. Earlier reports of improvement in bioavailability and retention of drugs upon nanoencapsulation have motivated us in developing various nanoformulations of curcumin, which were found to exhibit significant enhancement in bioavailability and retention time as assessed by our previous in vitro studies. Among the various formulations tested, curcumin-entrapped in PLGA-PEG nanoparticles conjugated to folic acid (PPF-curcumin) displayed maximum cell death. In the present study, we have demonstrated the efficacy of this formulation in augmenting the bioavailability and retention time of curcumin, in vivo, in Swiss albino mice. Further, the acute and chronic toxicity studies proved that the formulation is pharmacologically safe. We have also evaluated its potential in chemosensitizing cervical cancer cells to paclitaxel and have verified the results using cervical cancer xenograft model in NOD-SCID mice. Folic acid conjugation significantly enhanced the efficacy of curcumin in down-regulating various survival signals induced by paclitaxel in cervical cancer cells and have considerably improved its potential in inhibiting the tumor growth of cervical cancer xenografts. The non-toxic nature coupled with improved chemosensitization potential makes PPF-curcumin a promising candidate formulation for clinical trials.

8.
Sci Rep ; 6: 36318, 2016 11 03.
Article in English | MEDLINE | ID: mdl-27808117

ABSTRACT

We report, for the first time, the remarkable efficacy of uttroside B, a potent saponin from Solanum nigrum Linn, against liver cancer. The compound has been isolated and characterized from the leaves of Solanum nigrum Linn, a plant widely used in traditional medicine and is a rich resource of several anticancer molecules. Uttroside B, that comprises of ß-D-glucopyranosyl unit at C-26 of the furostanol and ß-lycotetraosyl unit at C-3, is ten times more cytotoxic to the liver cancer cell line, HepG2 (IC50: 0.5 µM) than sorafenib (IC50: 5.8 µM), the only FDA-approved drug for liver cancer. Moreover, it induces cytotoxicity in all liver cancer cell lines, irrespective of their HBV status, while being non-toxic to normal immortalized hepatocytes. It induces apoptosis in HepG2 cells by down-regulating mainly the activation of MAPK and mTOR pathways. The drastic reduction in HepG2-xenograft tumor size achieved by uttroside B in NOD-SCID mice and substantiation of its biological safety through both acute and chronic toxicity studies in Swiss albino mice warrants clinical validation of the molecule against hepatic cancer, for which, the chemotherapeutic armamentarium currently has limited weapons.


Subject(s)
Antineoplastic Agents, Phytogenic/administration & dosage , Carcinoma, Hepatocellular/drug therapy , Liver Neoplasms/drug therapy , Saponins/administration & dosage , Solanum nigrum/chemistry , TOR Serine-Threonine Kinases/metabolism , Animals , Antineoplastic Agents, Phytogenic/chemistry , Antineoplastic Agents, Phytogenic/pharmacology , Carcinoma, Hepatocellular/metabolism , Cell Proliferation/drug effects , Cell Survival/drug effects , Gene Expression Regulation, Neoplastic/drug effects , Hep G2 Cells , Humans , Liver Neoplasms/metabolism , MAP Kinase Signaling System/drug effects , Mice , Mice, Inbred NOD , Mice, SCID , Saponins/chemistry , Saponins/pharmacology , Xenograft Model Antitumor Assays
9.
Ann Med ; 48(3): 149-61, 2016.
Article in English | MEDLINE | ID: mdl-26911282

ABSTRACT

Human Papilloma Virus (HPV) is one of the most common sexually transmitted pathogen, globally. Oncogenic types of HPV are the causative agents of many neoplastic diseases, including cervical cancer, which ranks as the most common cancer affecting females in developing countries. HPV infection of the cervical epithelium and the subsequent integration of viral DNA into the host genome are the major risk factors for cervical cancer. The scientific discovery of HPV as the causal agent of cervical cancer has led to the development of HPV-based diagnostic tools. Prophylactic vaccines, based on the oncogenic HPV type virus-like particles have been introduced in several developed countries as a preliminary preventive approach. Nevertheless, it remains a continuous threat to women in developing countries, where the prophylactic vaccines are unaffordable and organized screening programmes are lacking. This warrants implementation of prevention strategies that will reduce cervical cancer-related mortality. In this review, we have discussed molecular pathogenesis of HPV infection and the risk factors associated with it. The diagnosis, treatment and prevention strategies of HPV-related cervical cancer have also been discussed.


Subject(s)
Oncogene Proteins, Viral/metabolism , Papillomaviridae/metabolism , Papillomavirus Infections , Sexually Transmitted Diseases/therapy , Uterine Cervical Neoplasms/therapy , DNA, Viral/isolation & purification , DNA, Viral/metabolism , Developing Countries , Disease Eradication/methods , Early Detection of Cancer/methods , Female , Humans , Mass Screening/methods , Papillomaviridae/genetics , Papillomaviridae/immunology , Papillomavirus Infections/complications , Papillomavirus Infections/diagnosis , Papillomavirus Infections/prevention & control , Papillomavirus Vaccines/therapeutic use , Prevalence , Risk Factors , Sexually Transmitted Diseases/diagnosis , Sexually Transmitted Diseases/prevention & control , Sexually Transmitted Diseases/virology , Uterine Cervical Neoplasms/diagnosis , Uterine Cervical Neoplasms/prevention & control , Uterine Cervical Neoplasms/virology
10.
Biofactors ; 41(6): 431-42, 2015.
Article in English | MEDLINE | ID: mdl-26643788

ABSTRACT

Benzo[a]pyrene is a procarcinogen present in environment and cigarette smoke, which could be bio-transformed in vivo to B[a]PDE, a potent carcinogen known to form DNA adducts and induce mutations. We observed that curcumin, a known chemopreventive, could significantly inhibit the survival of lung cancer cells exposed to B[a]PDE. It also downregulates B[a]PDE-induced nuclear translocation of NF-κB as assessed by Electrophoretic Mobility Shift Assay (EMSA) and NF-κB-dependent reporter gene assay. Ames assay demonstrated its ability to revert the mutagenic property of benzo[a]pyrene. These observations prompted us to evaluate the efficacy of curcumin in preventing B[a]P-induced lung carcinogenesis in vivo and to explore the molecular mechanism associated with it. The average number of tumor nodules present in the lungs of the Swiss albino mice, which received benzo[a]pyrene, was significantly high compared to that received curcumin as 2% diet along with B[a]P. Curcumin treatment significantly reverted histopathological deviations in the lung tissues due to benzo[a]pyrene ingestion. Moreover, curcumin diet reduced benzo[a]pyrene-induced activation of NF-κB and MAPK signaling and Cox-2 transcription in lung tissues of mice. Taken together, this study illustrates multifaceted efficacy of curcumin in preventing lung cancer.


Subject(s)
Carcinogenesis/genetics , Curcumin/administration & dosage , Lung Neoplasms/diet therapy , Lung Neoplasms/genetics , 7,8-Dihydro-7,8-dihydroxybenzo(a)pyrene 9,10-oxide/toxicity , Animals , Benzo(a)pyrene/toxicity , Biotransformation , Carcinogenesis/drug effects , DNA Adducts/drug effects , Humans , Lung Neoplasms/chemically induced , Lung Neoplasms/pathology , Mice , Mutagenesis/drug effects , Mutagenesis/genetics , NF-kappa B/genetics
11.
PLoS One ; 9(8): e104401, 2014.
Article in English | MEDLINE | ID: mdl-25157570

ABSTRACT

We report mechanism-based evidence for the anticancer and chemopreventive efficacy of [6]-gingerol, the major active principle of the medicinal plant, Ginger (Zingiber officinale), in colon cancer cells. The compound was evaluated in two human colon cancer cell lines for its cytotoxic effect and the most sensitive cell line, SW-480, was selected for the mechanistic evaluation of its anticancer and chemopreventive efficacy. The non-toxic nature of [6]-gingerol was confirmed by viability assays on rapidly dividing normal mouse colon cells. [6]-gingerol inhibited cell proliferation and induced apoptosis as evidenced by externalization of phosphatidyl serine in SW-480, while the normal colon cells were unaffected. Sensitivity to [6]-gingerol in SW-480 cells was associated with activation of caspases 8, 9, 3 &7 and cleavage of PARP, which attests induction of apoptotic cell death. Mechanistically, [6]-gingerol down-regulated Phorbol Myristate Acetate (PMA) induced phosphorylation of ERK1/2 and JNK MAP kinases and activation of AP-1 transcription factor, but had only little effects on phosphorylation of p38 MAP kinase and activation of NF-kappa B. Additionally, it complemented the inhibitors of either ERK1/2 or JNK MAP kinase in bringing down the PMA-induced cell proliferation in SW-480 cells. We report the inhibition of ERK1/2/JNK/AP-1 pathway as a possible mechanism behind the anticancer as well as chemopreventive efficacy of [6]-gingerol against colon cancer.


Subject(s)
Anticarcinogenic Agents/pharmacology , Antineoplastic Agents, Phytogenic/pharmacology , Catechols/pharmacology , Colonic Neoplasms/drug therapy , Extracellular Signal-Regulated MAP Kinases/metabolism , Fatty Alcohols/pharmacology , JNK Mitogen-Activated Protein Kinases/metabolism , Transcription Factor AP-1/metabolism , Anticarcinogenic Agents/chemistry , Antineoplastic Agents, Phytogenic/chemistry , Apoptosis/drug effects , Carcinogens/toxicity , Caspases/metabolism , Catechols/chemistry , Cell Line, Tumor , Colon/drug effects , Colon/metabolism , Colonic Neoplasms/chemically induced , Colonic Neoplasms/metabolism , Colonic Neoplasms/prevention & control , Fatty Alcohols/chemistry , Zingiber officinale/chemistry , Humans , Signal Transduction/drug effects , Tetradecanoylphorbol Acetate/toxicity
12.
IMA Fungus ; 4(2): 259-63, 2013 Dec.
Article in English | MEDLINE | ID: mdl-24563838

ABSTRACT

The Structural and Biochemical Database (SBD), developed as part of the US NSF-funded Assembling the Fungal Tree of Life (AFTOL), is a multi-investigator project. It is a major resource to present and manage morphological and biochemical information on Fungi and serves as a phyloinformatics tool for the scientific community. It also is an important resource for teaching mycology. The database, available at http://aftol.umn.edu, includes new and previously published subcellular data on Fungi, supplemented with images and literature links. Datasets automatically combined in NEXUS format from the site permit independent and combined (with molecular data) phylogenetic analyses. Character lists, a major feature of the site, serve as primary reference documents of subcellular and biochemical characters that distinguish taxa across the major fungal lineages. The character lists illustrated with images and drawings are informative for evolutionary and developmental biologists as well as educators, students and the public. Fungal Subcellular Ontology (FSO), developed as part of this effort is a primary initiative to provide a controlled vocabulary describing subcellular structures unique to Fungi. FSO establishes a full complement of terms that provide an operating ontological framework for the database. Examples are provided for using the database for teaching.

13.
Int J Nanomedicine ; 7: 4077-88, 2012.
Article in English | MEDLINE | ID: mdl-22888244

ABSTRACT

OBJECTIVE: To investigate cross-linked hydrogels prepared via inverse emulsion polymerization to entrap poorly aqueous soluble drugs. Polyethylene glycol cross-linked acrylic polymers were synthesized and the loading and release of curcumin, a model hydrophobic drug, was investigated. METHODS: Physicochemical characteristics of hydrogels were studied with (13)C nuclear magnetic resonance, Fourier transform infrared spectroscopy, transmission electron microscopy, scanning electron microscopy, differential scanning calorimetry, and swelling. Polymerization of the acrylic acid with cross-linked polyethylene glycol diacrylate was characterized with (13)C nuclear magnetic resonance imaging and Fourier transform infrared spectroscopy. RESULTS: The in vitro release rate of curcumin showed that there was a sustained release from the hydrogel with increased cross-linking; the release rate depended on the pH of the releasing medium. Intracellular and cytotoxicity studies were carried out in human cervical cancer cell lines. CONCLUSION: The results suggest cross-linked acrylic polymers can be used as efficient vectors for pH-sensitive, controlled delivery of hydrophobic drugs.


Subject(s)
Acrylates/chemistry , Antineoplastic Agents/administration & dosage , Drug Delivery Systems/methods , Hydrogels/chemistry , Nanostructures/chemistry , Polyethylene Glycols/chemistry , Acrylates/administration & dosage , Antineoplastic Agents/chemistry , Antineoplastic Agents/pharmacokinetics , Apoptosis/drug effects , Cell Cycle Checkpoints/drug effects , Cell Survival/drug effects , Curcumin/administration & dosage , Curcumin/chemistry , Curcumin/pharmacokinetics , Dimethyl Sulfoxide , Down-Regulation/drug effects , HeLa Cells , Humans , Hydrogen-Ion Concentration , Hydrophobic and Hydrophilic Interactions , Nanostructures/administration & dosage , Particle Size , Polyethylene Glycols/administration & dosage , Spectroscopy, Fourier Transform Infrared
14.
Int J Pharm ; 425(1-2): 44-52, 2012 Apr 04.
Article in English | MEDLINE | ID: mdl-22266528

ABSTRACT

Curcumin, a yellow pigment present in turmeric, possess potential anti-proliferative and anti-inflammatory activities but poor aqueous solubility limits its applications. In this study we report a novel comparative study of the formulation and characterization of curcumin nanoparticles (nanocurcumin) using two poly (lactide-co-glycolide) (PLGA) combinations, 50:50 and 75:25 having different lactide to glycolide ratios. Nanocurcumin 50:50 showed smaller size with higher encapsulation efficiency. Thermal evaluation suggested the presence of curcumin in molecular dispersion form which supported its sustained release up to a week where nanocurcumin 50:50 showed faster release. Cellular uptake studies in human epithelial cervical cancer cells (HeLa) exhibited enhanced intracellular fluorescence with nanocurcumin when compared to free curcumin, when both given in purely aqueous media. Antiproliferative studies using MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay, Annexin V/propidium iodide staining, poly (ADP-ribose) polymerase (PARP) cleavage and downregulation of clonogenic potential of HeLa cells proved the better antitumor activity of nanocurcumin 50:50 administered in aqueous media. Superior efficacy of nanocurcumin 50:50 in comparison to free curcumin was further demonstrated by electrophoretic mobility shift assay and immunocytochemical analysis. In conclusion, the enhanced aqueous solubility and higher anticancer efficacy of nanocurcumin administered in aqueous media clearly demonstrates its potential against cancer chemotherapy, with dependence on the combination of PLGA.


Subject(s)
Antineoplastic Agents, Phytogenic/administration & dosage , Curcumin/administration & dosage , Drug Carriers/administration & dosage , Lactic Acid/administration & dosage , Nanoparticles/administration & dosage , Polyglycolic Acid/administration & dosage , Antineoplastic Agents, Phytogenic/chemistry , Cell Survival/drug effects , Curcumin/chemistry , Drug Carriers/chemistry , HeLa Cells , Humans , Lactic Acid/chemistry , Microscopy, Electron, Transmission , Nanoparticles/chemistry , Nanoparticles/ultrastructure , Poly(ADP-ribose) Polymerases/metabolism , Polyglycolic Acid/chemistry , Polylactic Acid-Polyglycolic Acid Copolymer , Transcription Factor RelA/metabolism
15.
Int J Biochem Cell Biol ; 43(3): 331-41, 2011 Mar.
Article in English | MEDLINE | ID: mdl-20883815

ABSTRACT

Paclitaxel is the most promising chemotherapeutic agent of plant origin despite its high cost and dose-limiting toxicity. Our earlier report has shown that cervical cancer cells can be sensitized by curcumin to paclitaxel-induced apoptosis through down-regulation of NF-κB and Akt. In the present study we have attempted to decipher the signaling pathways regulating the synergism of paclitaxel and curcumin. The study has clearly proved that Akt and NF-κB function successively in the sequence of paclitaxel induced signaling events where Akt is upstream of NF-κB. While inhibition of NF-κB led to complete inhibition of the synergism of paclitaxel and curcumin, inhibition of Akt brought about only partial reduction of the same, suggesting that, apart from Akt, there are other pathways induced by paclitaxel leading to NF-κB activation, which are also down-regulated by curcumin. Inactivation of NF-κB did not affect the activation of Akt and survivin, while that of Akt significantly inhibited NF-κB and completely inhibited up-regulation of survivin. Up-regulation of Cyclin-D1, Cox-2, XIAP and cIAP1 and phosphorylation of MAPKs, were completely inhibited on inactivation of NF-κB assigning a key regulatory role to NF-κB in the synergistic effect of paclitaxel and curcumin. While up-regulation of survivin by paclitaxel is regulated by Akt, independent of NF-κB, inactivation of neither Akt nor NF-κB produced any change in Bcl-2 level suggesting a distinct pathway for its action. As curcumin could effectively down-regulate all these survival signals induced by paclitaxel, we suggest it as a potent chemosensitizer to improve the therapeutic index of paclitaxel.


Subject(s)
Curcumin/pharmacology , Down-Regulation/drug effects , Mitogen-Activated Protein Kinases/metabolism , NF-kappa B/metabolism , Paclitaxel/pharmacology , Proto-Oncogene Proteins c-akt/metabolism , Signal Transduction/drug effects , Cell Cycle/drug effects , Cell Survival/drug effects , Cyclin D1/genetics , Cyclin D1/metabolism , Cyclooxygenase 2/genetics , Cyclooxygenase 2/metabolism , Drug Synergism , Enzyme Activation/drug effects , Gene Expression Regulation, Neoplastic/drug effects , HeLa Cells , Humans , Inhibitor of Apoptosis Proteins/metabolism , Models, Biological , Proto-Oncogene Proteins c-bcl-2/metabolism , Survivin , Transcription Factor AP-1/metabolism
16.
Mol Cancer ; 9: 220, 2010 Aug 20.
Article in English | MEDLINE | ID: mdl-20727180

ABSTRACT

BACKGROUND: Lung cancer is the most lethal cancer and almost 90% of lung cancer is due to cigarette smoking. Even though nicotine, one of the major ingredients of cigarette smoke and the causative agent for addiction, is not a carcinogen by itself, several investigators have shown that nicotine can induce cell proliferation and angiogenesis. We observed that the proliferative index of nicotine is different in the lung cancer cell lines H1299 (p53-/-) and A549 (p53+/+) which indicates that the mode of up-regulation of survival signals by nicotine might be different in cells with and without p53. RESULTS: While low concentrations of nicotine induced activation of NF-κB, Akt, Bcl2, MAPKs, AP1 and IAPs in H1299, it failed to induce NF-κB in A549, and compared to H1299, almost 100 times higher concentration of nicotine was required to induce all other survival signals in A549. Transfection of WT-p53 and DN-p53 in H1299 and A549 respectively, reversed the mode of activation of survival signals. Curcumin down-regulated all the survival signals induced by nicotine in both the cells, irrespective of their p53 status. The hypothesis was confirmed when lower concentrations of nicotine induced NF-κB in two more lung cancer cells, Hop-92 and NCI-H522 with mutant p53 status. Silencing of p53 in A549 using siRNA made the cells susceptible to nicotine-induced NF-κB nuclear translocation as in A549 DN-p53 cells. CONCLUSIONS: The present study reveals a detrimental role of nicotine especially in lung cancer patients with impaired p53 status and identifies curcumin as a potential chemopreventive.


Subject(s)
Curcumin/pharmacology , Down-Regulation/drug effects , Lung Neoplasms/metabolism , Nicotine/pharmacology , Signal Transduction/drug effects , Tumor Suppressor Protein p53/metabolism , Cell Line, Tumor , Cell Proliferation/drug effects , Cyclin D1/metabolism , Cyclooxygenase 2/metabolism , Humans , Lung Neoplasms/pathology , Phosphorylation , Proto-Oncogene Proteins c-akt/metabolism , Transcription Factor AP-1/metabolism
17.
J Phys Condens Matter ; 21(50): 505103, 2009 Dec 16.
Article in English | MEDLINE | ID: mdl-21836225

ABSTRACT

We report the observation of mostly wedge disclinations of strength ± 1/2 in a uniaxial nematic liquid crystal. The dense network of the disclination is stabilized in cells of thickness (∼6 µm) treated with perfluoropolymer. The distribution of net defect strength was found to be Gaussian. The scaling exponent obtained from the width of the distribution is ν = 0.29 ± 0.08 and is in good agreement with the prediction based on the cosmological Kibble mechanism. The exponent and the constant of the scaling relation are compared with the values reported for lyotropic liquid crystal with half-strength disclination by Mukai and co-workers.

18.
Conf Proc IEEE Eng Med Biol Soc ; 2005: 1468-71, 2005.
Article in English | MEDLINE | ID: mdl-17282477

ABSTRACT

The surface backscattered radiations of curved tissue-equivalent phantom are measured using miniature multi-probe laser reflectometer imaging system. Phantom models are prepared using paraffin wax mixed with wax colors and their optical parameters are determined by comparing measured backscattered profile with that of Monte Carlo Simulation procedure. Abnormalities with optical parameters 5% less than the normal phantom are introduced at various depths in different locations. These phantoms are scanned using miniature laser reflectometer scanner. The acquired data after digitizing, interpolation and filtering is represented as 3-D color coded images which show the location and size of the abnormalities.

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