Preeti Nagar
Post Doctoral Fellow
postdoc
Biochemistry & Molecular Biology, College of Medicine
Research Areas
Biography and Research Information
OverviewAI-generated summary
Preeti Nagar's research investigates molecular mechanisms underlying plant stress responses and their applications in agriculture, as well as the role of molecular pathways in human cancer development. Her work on plants includes studying the function of phytosulfokine receptors in enhancing abscisic acid response and drought stress tolerance in rice, and their role in leaf senescence and reactive oxygen species signaling in *Arabidopsis thaliana*. Nagar has also examined transcript profiling of Polycomb gene families in *Oryza sativa* to understand abiotic stress responses. In the realm of human health, her research focuses on the involvement of nonsense-mediated mRNA decay in tumorigenesis and the impact of the NONO protein on breast cancer cell pathways. She has also explored RNA splicing in cancer and its potential for targeted therapies, including the role of SRSF6 and SRSF1 in human gene regulation relevant to cancer.
Metrics
- h-index: 11
- Publications: 22
- Citations: 452
Selected Publications
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Mitochondrial antioxidant enzyme (SOD2) at the crossroads of redox signaling and cancer progression (2026)
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Genetics behind aflatoxin biosynthesis and tolerance in crops (2026)
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Targeting <i>EZH2</i> Oncogenic Splicing: Decoding the Regulatory Network and Antisense Correction (2026)
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SRSF6 and SRSF1 coordinately enhance the inclusion of human <i>MUSK</i> exon 10 to generate a Wnt-sensitive MuSK isoform (2025)
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Beyond the Sin3/HDAC Complex: FAM60A emerges as a regulator of RNA Splicing (2024)
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RNA Splicing in Cancer and Targeted Therapies (2023)
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Nonsense-Mediated mRNA Decay as a Mediator of Tumorigenesis (2023)
Grants & Funding
- Center for Molecular Interactions in Cancer (CMIC) NIH Co-Investigator
Collaboration Network
Top Collaborators
- Nonsense-Mediated mRNA Decay as a Mediator of Tumorigenesis
- SRSF6 and SRSF1 coordinately enhance the inclusion of human <i>MUSK</i> exon 10 to generate a Wnt-sensitive MuSK isoform
- RNA Splicing in Cancer and Targeted Therapies
- Beyond the Sin3/HDAC Complex: FAM60A emerges as a regulator of RNA Splicing
- Targeting <i>EZH2</i> Oncogenic Splicing: Decoding the Regulatory Network and Antisense Correction
- <scp>OsPSKR15</scp>, a phytosulfokine receptor from rice enhances abscisic acid response and drought stress tolerance
- Transcript profiling of Polycomb gene family in Oryza sativa indicates their abiotic stress-specific response
- Phytosulfokine receptor 1 (AtPSKR1) acts as a positive regulator of leaf senescence by mediating ROS signaling in Arabidopsis thaliana
- Unveiling the molecular mechanism underlying PSKR-mediated amplification of the ABA signaling in Arabidopsis thaliana
- Nonsense-Mediated mRNA Decay as a Mediator of Tumorigenesis
- SRSF6 and SRSF1 coordinately enhance the inclusion of human <i>MUSK</i> exon 10 to generate a Wnt-sensitive MuSK isoform
- RNA Splicing in Cancer and Targeted Therapies
- Beyond the Sin3/HDAC Complex: FAM60A emerges as a regulator of RNA Splicing
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octamer-Binding (NONO) Protein Stability Regulated by PIN1 is Crucial for Breast Cancer Tumorigenicity Via the MAPK/β-Catenin Pathway
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octamer-Binding (NONO) Protein Stability Regulated by PIN1 is Crucial for Breast Cancer Tumorigenicity Via the MAPK/β-Catenin Pathway
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octamer-Binding (NONO) Protein Stability Regulated by PIN1 is Crucial for Breast Cancer Tumorigenicity Via the MAPK/β-Catenin Pathway
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octamer-Binding (NONO) Protein Stability Regulated by PIN1 is Crucial for Breast Cancer Tumorigenicity Via the MAPK/β-Catenin Pathway
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octamer-Binding (NONO) Protein Stability Regulated by PIN1 is Crucial for Breast Cancer Tumorigenicity Via the MAPK/β-Catenin Pathway
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Transcript profiling of Polycomb gene family in Oryza sativa indicates their abiotic stress-specific response
- Phytosulfokine receptor 1 (AtPSKR1) acts as a positive regulator of leaf senescence by mediating ROS signaling in Arabidopsis thaliana
- Unveiling the molecular mechanism underlying PSKR-mediated amplification of the ABA signaling in Arabidopsis thaliana
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cells
- Non-POU Domain-Containing Octomer-Binding (NONO) protein expression and stability promotes the tumorigenicity and activation of Akt/MAPK/β-catenin pathways in human breast cancer cell Running title: NONO promotes the tumorigenicity of breast cancer
- Phytosulfokine receptor 1 (AtPSKR1) acts as a positive regulator of leaf senescence by mediating ROS signaling in Arabidopsis thaliana
- Unveiling the molecular mechanism underlying PSKR-mediated amplification of the ABA signaling in Arabidopsis thaliana
- SRSF6 and SRSF1 coordinately enhance the inclusion of human <i>MUSK</i> exon 10 to generate a Wnt-sensitive MuSK isoform
- Targeting <i>EZH2</i> Oncogenic Splicing: Decoding the Regulatory Network and Antisense Correction
- SRSF6 and SRSF1 coordinately enhance the inclusion of human <i>MUSK</i> exon 10 to generate a Wnt-sensitive MuSK isoform
- Targeting <i>EZH2</i> Oncogenic Splicing: Decoding the Regulatory Network and Antisense Correction
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