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1.
Protein & Cell ; (12): 178-190, 2017.
Article in English | WPRIM | ID: wpr-757374

ABSTRACT

Lung cancer is the leading cause of cancer-related deaths worldwide. Targeted therapy is beneficial in most cases, but the development of drug resistance stands as an obstacle to good prognosis. Multiple mechanisms were explored such as genetic alterations, activation of bypass signaling, and phenotypic transition. These intrinsic and/or extrinsic dynamic regulations facilitate tumor cell survival in meeting the demands of signaling under different stimulus. This review introduces lung cancer plasticity and heterogeneity and their correlation with drug resistance. While cancer plasticity and heterogeneity play an essential role in the development of drug resistance, the manipulation of them may bring some inspirations to cancer prognosis and treatment. That is to say, lung cancer plasticity and heterogeneity present us with not only challenges but also opportunities.


Subject(s)
Humans , Carcinoma, Non-Small-Cell Lung , Genetics , Metabolism , Drug Resistance, Neoplasm , Genetics , Lung Neoplasms , Genetics , Metabolism
2.
Chinese Journal of Biotechnology ; (12): 1679-1690, 2014.
Article in Chinese | WPRIM | ID: wpr-345555

ABSTRACT

In order to determine immunogenicity and protective effect in chickens, we used the IBDV (Infectious bursal disease virus)-Vp2/Lactobacillus casei as antigen transfer system. First, the immunized and control chickens were challenged by IBDV/DQ at lethal dose to determine the protective ratio. Second, chickens were orallyand intranasally vaccinated twice with 10(9) CFU/mL pLA-VP2/L. casei, pLA/L. casei and PBS as negativecontrol and commercial vaccine as positive control. The bursa injury and the lesion score wererecorded post challenge. The level of specific IgG and sIgA in pLA-VP2/L. casei and positive control groups was significantly higher than that in negativecontrol groups. The protection efficacy in pLA-VP2/L. casei oral group was higher than that inintranasal group. The SI. of pLA-VP2/L. casei oral group was significant higher than other groups. The lesion score indicated the pLA-VP2/L. casei was safer than commercial vaccine for bursa. Collectively, the pLA-VP2/L. casei could be a vaccine candidate for IBDV.


Subject(s)
Animals , Antibodies, Viral , Blood , Antibody Formation , Birnaviridae Infections , Chickens , Infectious bursal disease virus , Lacticaseibacillus casei , Poultry Diseases , Recombinant Proteins , Allergy and Immunology , Viral Structural Proteins , Allergy and Immunology , Viral Vaccines , Allergy and Immunology
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