mpn-research-assistant

---

name: mpn-research-assistant description: "Myeloproliferative neoplasm (MPN) research expertise including JAK2/CALR/MPL mutations, myelofibrosis, polycythemia vera, essential thrombocythemia. Use for MPN literature search, driver mutation analysis, PPM1D pathway analysis, fibrosis markers, megakaryocyte biology, clinical trial data interpretation, and translational research." license: Proprietary

MPN Research Assistant

Disease Classification

WHO 2022 Classification

• Polycythemia Vera (PV): JAK2V617F (95%), JAK2 exon 12 (3%)
• Essential Thrombocythemia (ET): JAK2V617F (55%), CALR (25%), MPL (5%)
• Primary Myelofibrosis (PMF): JAK2V617F (55%), CALR (25%), MPL (8%)
• Pre-PMF: Early fibrotic stage, better prognosis
• Overt PMF: Grade 2-3 fibrosis, splenomegaly

Driver Mutations

Mutation	Gene Location	Mechanism	VAF Significance
JAK2V617F	9p24.1	Constitutive JAK-STAT activation	>50% → poor prognosis
CALR (type 1)	19p13.2	52bp deletion, MPL activation	Better prognosis
CALR (type 2)	19p13.2	5bp insertion, MPL activation	Intermediate
MPL W515L/K	1p34.2	TPO-independent signaling	Thrombocytosis

High Molecular Risk (HMR) Mutations

• ASXL1, EZH2, SRSF2, IDH1/2, U2AF1
• ≥2 HMR mutations = very high risk

PPM1D Pathway Analysis

Expression Patterns

• 83.9-fold overexpression vs normal donors (p=0.0002)
• JAK2V617F+ > CALR+ expression (43.4x vs 13.4x, p=0.01)
• Mutation frequency: 1.9% (8th most common in MPNs)

Therapeutic Targets

ppm1d_targets = {
    'PPM1D inhibitors': ['GSK2830371', 'SL-176'],
    'MDM2 inhibitors': ['navtemadlin (KRT-232)', 'idasanutlin'],
    'Combination': ['PPM1D + MDM2 (synergistic)'],
}

# p53 pathway restoration
mechanism = """
PPM1D inhibition → ↑p53 phosphorylation →
↑p53 stabilization → ↑DNA damage response →
↑apoptosis in mutant clones
"""

Clinical Trial Data (BOREAS)

• Navtemadlin: 15% SVR35, 24% TSS50
• CD34+ reduction: 68-76% at 24-36 weeks
• VAF reduction: 21% achieved ≥50% decrease
• Fibrosis improvement: 45% by one grade

Megakaryocyte Subtypes in MPNs

mk_subtypes = {
    'Endomitotic MKs': {
        'markers': ['ITGA2B', 'GP1BA', 'PF4', 'TUBB1'],
        'function': 'Polyploidization',
        'mpn_change': 'Dysregulated endomitosis'
    },
    'Platelet-Generating MKs': {
        'markers': ['VWF', 'F2R', 'GP9', 'SELP'],
        'function': 'Proplatelet formation',
        'mpn_change': 'Abnormal platelet production'
    },
    'HSC Niche-Supporting MKs': {
        'markers': ['THPO', 'IGF1', 'CXCL12', 'ANGPT1'],
        'function': 'HSC maintenance',
        'mpn_change': 'Disrupted niche signaling'
    },
    'Inflammatory MKs': {
        'markers': ['S100A8', 'S100A9', 'CHI3L1', 'CXCL8'],
        'function': 'Inflammation',
        'mpn_change': 'Expanded in MF'
    }
}

Fibrosis Markers

Psaila 2020 Fibrosis Gene Signature

fibrosis_genes = [
    'TGFB1', 'IL12A', 'IL1B', 'RAB37', 'TIMP1', 'APIP', 'PF4V1', 'VEGFA',
    'FBLN2', 'SFRP1', 'COL6A2', 'COL4A2', 'COL5A1', 'PDGFRB', 'LOXL2', 'RUNX2'
]

# ECM remodeling
ecm_markers = ['COL1A1', 'COL3A1', 'FN1', 'LAMA1', 'LAMB1']

# Profibrotic cytokines
cytokines = ['TGFB1', 'PDGF', 'VEGFA', 'IL1B', 'IL6', 'TNF']

Prognostic Scoring Systems

MIPSS70+ v2.0 (Myelofibrosis)

Variable	Points
Hemoglobin <10 g/dL	2
Blasts ≥2%	1
Constitutional symptoms	2
Absence of CALR type-1	2
HMR mutations	2 each
Unfavorable karyotype	3

Risk Categories

• Very Low: 0-1 points (10yr OS: 92%)
• Low: 2-4 points
• Intermediate: 5-8 points
• High: 9-11 points
• Very High: ≥12 points

Data Integration Template

def create_mpn_patient_matrix(clinical_df, mutations_df,
                               cytokines_df, flow_df, degs_df):
    """Integrate multi-modal MPN patient data."""

    # Merge clinical
    matrix = clinical_df.copy()

    # Add mutation status
    driver_muts = ['JAK2', 'CALR', 'MPL']
    hmr_muts = ['ASXL1', 'EZH2', 'SRSF2', 'IDH1', 'IDH2']

    for mut in driver_muts + hmr_muts:
        if mut in mutations_df.columns:
            matrix[f'{mut}_status'] = mutations_df[mut]

    # Calculate HMR count
    matrix['HMR_count'] = matrix[[f'{m}_status' for m in hmr_muts
                                   if f'{m}_status' in matrix.columns]].sum(axis=1)

    # Add cytokine data
    for cyto in ['TGFB1', 'IL6', 'IL8']:
        if cyto in cytokines_df.columns:
            matrix[f'{cyto}_level'] = cytokines_df[cyto]

    # Add flow cytometry
    matrix['CD34_percent'] = flow_df['CD34_positive_percent']

    return matrix

Key References

key_papers = {
    'Williams_2022': 'Blood: Phylogenetic reconstruction of MPN evolution',
    'Psaila_2020': 'Nature Medicine: Single-cell profiling of MF megakaryocytes',
    'Mascarenhas_2022': 'Blood Advances: Idasanutlin in PV',
    'BOREAS_2024': 'Phase III navtemadlin in MF',
    'Marcellino_iPSC': 'PPM1D iPSC modeling in MPNs',
    'Kanagal-Shamanna': 'Mod Pathol: i(17q) in MDS/MPN'
}

PubMed Search Templates

mpn_search_queries = {
    'ppm1d_mpn': '"PPM1D"[Title/Abstract] AND ("myeloproliferative"[Title/Abstract] OR "myelofibrosis"[Title/Abstract])',
    'single_cell_mpn': '"single-cell"[Title/Abstract] AND "myeloproliferative neoplasm"[Title/Abstract]',
    'jak2_calr': '(JAK2V617F OR "CALR mutation") AND myeloproliferative',
    'fibrosis_mk': 'megakaryocyte[Title/Abstract] AND fibrosis[Title/Abstract] AND myelofibrosis'
}

See references/mpn_clinical_trials.md for ongoing trials. See references/mpn_mutations_database.md for complete mutation catalog.