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. Author manuscript; available in PMC: 2017 Jan 3.
Published in final edited form as: Nat Rev Clin Oncol. 2012 Sep 11;9(11):643–653. doi: 10.1038/nrclinonc.2012.156

Figure 1.

Figure 1

Targeted therapy of lymphoma. a | Although targeting the underlying driver oncogenic process is logical, recent progress in lymphoma therapy has resulted from targeting non-oncogenic proteins, such as CD20 and CD30. b | Hundreds of genetic alterations in tumour cells have been identified in tumour-suppressor genes or oncogenes. Rather than designing unique drugs for each genetic alteration, several genetic defects can be grouped within well-defined oncogenic pathways. Such an approach may simplify drug development as only a dozen or so oncogenic pathways have been described. Within each pathway, multiple proteins can be targeted, regardless of their mutation status.