Kuljanin Miljan M

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Proteomics (3)

Organisms

NEWT:188908 (3)
Actinidia deliciosa (3)
Rosa hybrid cultivar (3)
NEWT:391290 (3)
Norwalk virus (3)
NEWT:1051067 (3)
NEWT:85310 (3)
NEWT:637616 (3)
NEWT:8040 (3)
Dinothrombium (3)
Pseudomonas fragi (3)
NEWT:1634342 (3)
Fusarium oxysporum f. sp. vasinfectum 25433 (3)
NEWT:1354724 (3)
NEWT:82076 (3)
Halyomorpha halys (3)
Norovirus Hu/GII-4/Saga4/2006/JP (3)
NEWT:86185 (3)
NEWT:299467 (3)
NEWT:1608994 (3)
Pseudotsuga menziesii (3)
Cryptosporidium parvum Iowa (3)
NCBITaxon:11292 (3)
NEWT:189513 (3)
NEWT:139 (3)
Culex pipiens molestus (3)
NEWT:5874 (3)
Influenza A virus (A/India/P063078/2006(H3N2)) (3)
NEWT:2749149 (3)
NCBITaxon:11082 (3)

Repository

pride (3)

Tissue

Pancreatic ductal cell (1)
Spleen (1)
Epithelial cell (1)
Cell culture (1)

Disease

Pancreatic cancer (1)

Technology Type

Mass Spectrometry (3)
Shotgun proteomics (2)
Bottom-up proteomics (1)

Publication Date

2025 (1)
2022 (1)
2021 (1)

Lab affiliation

Division of Genomic Stability and DNA Repair, Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA 02215, USA, Hale Family Pancreatic Cancer Research Center, Dana-Farber Cancer Institute, Boston, MA 02215, USA (1)
Division of Radiation and Genome Stability, Department of Radiation Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA Department of Radiation Oncology, Brigham and Women’s Hospital, Boston, MA 02115 (1)
Department of Cell Biology, Harvard Medical School, Boston MA, USA (1)

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Neurons Release Serine to Support mRNA Translation in Pancreatic Cancer

Pancreatic ductal adenocarcinoma (PDAC) tumors have a nutrient-poor, desmoplastic, and highly innervated tumor microenvironment. Although neurons can release stimulatory factors to accelerate PDAC tumorigenesis, the metabolic contribution of peripheral axons has not been explored. We found that peri...

ORGANISM(S): Homo sapiens (Human)

2025-07-07 | PXD064874 | Pride

Reimagining high-throughput profiling of reactive cysteines for cell-based screening of large electrophile libraries

Current methods for measuring amino-acid side-chain reactivity lack the throughput needed to screen large chemical libraries for interactions across the proteome. Here we redesigned the workflow for activity-based protein profiling of reactive cysteine residues by using a smaller desthiobiotin-based...

ORGANISM(S): Homo sapiens (Human) Mus musculus (Mouse)

2021-01-26 | PXD022511 | Pride

Reactive cysteines Chemical proteomics

NCOA4-mediated ferritinophagy is a pancreatic cancer dependency via maintenance of iron bioavailability for iron-sulfur cluster proteins

Oncogenic KRAS rewires pancreatic ductal adenocarcinoma (PDAC) metabolism to promote dependence on autophagy and iron metabolism. NCOA4-mediated ferritinophagy links autophagy and iron metabolism as NCOA4 selectively targets ferritin, the cellular iron storage complex, via autophagy to the lysosome ...