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"B-cell lymphoma cell proliferation" refers to the abnormal multiplication of malignant B lymphocytes, a hallmark of diseases such as diffuse large B-cell lymphoma (DLBCL). This process is driven by dysregulation of key oncogenes and tumor suppressor genes (e.g., MYC, BCL2, BCL6) through genetic mutations, translocations, or aberrant signaling pathways. As a process, it is targeted therapeutically by agents acting on the underlying molecular drivers, not as a single targetable protein or receptor. Precise therapeutic strategies require identification of the driving mutations or proteins that regulate this proliferation.[1][2][3][4]
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