A recent report in The New England Journal of Medicine by Liao and colleagues highlights the benefit of aspirin use in a molecular defined subgroup of patients affected by metastatic colorectal cancer (CRC). Authors concluded that it is very likely that the regular use of aspirin after CRC diagnosis is associated with longer survival among patients with mutated-PIK3CA tumors. In contrast, aspirin has no effect on cancer-specific survival in patients with wild-type PIK3CA CRC (1). The phosphatidylinositol 3-kinase (PI3K) signaling pathway plays an important role in carcinogenesis of CRC. Activating mutations in PIK3CA occur in two “hotspots” located in exon 9 (E542K, E545K) and exon 20 (H1047R) in approximately 15% of CRCs (2). PIK3CA encodes for a lipid kinase that regulates signaling pathways downstream of the Epidermal Growth Factor Receptor (EGFR), and its mutations hamper sensitivity to the anti-EGFR monoclonal antibodies cetuximab or panitumumab registered for metastatic CRC treatment (3,4).

Aspirin for colorectal cancer with PIK3CA mutations : the rising of the oldest targeted therapy? / A. Amatu, K. Bencardino, A. Sartore Bianchi, S. Siena. - In: ANNALS OF TRANSLATIONAL MEDICINE. - ISSN 2305-5839. - 1:2(2013 Jul), p. 12. [10.3978/j.issn.2305-5839.2013.01.03]

Aspirin for colorectal cancer with PIK3CA mutations : the rising of the oldest targeted therapy?

A. Sartore Bianchi;S. Siena
Ultimo
2013

Abstract

A recent report in The New England Journal of Medicine by Liao and colleagues highlights the benefit of aspirin use in a molecular defined subgroup of patients affected by metastatic colorectal cancer (CRC). Authors concluded that it is very likely that the regular use of aspirin after CRC diagnosis is associated with longer survival among patients with mutated-PIK3CA tumors. In contrast, aspirin has no effect on cancer-specific survival in patients with wild-type PIK3CA CRC (1). The phosphatidylinositol 3-kinase (PI3K) signaling pathway plays an important role in carcinogenesis of CRC. Activating mutations in PIK3CA occur in two “hotspots” located in exon 9 (E542K, E545K) and exon 20 (H1047R) in approximately 15% of CRCs (2). PIK3CA encodes for a lipid kinase that regulates signaling pathways downstream of the Epidermal Growth Factor Receptor (EGFR), and its mutations hamper sensitivity to the anti-EGFR monoclonal antibodies cetuximab or panitumumab registered for metastatic CRC treatment (3,4).
Settore MED/06 - Oncologia Medica
lug-2013
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/423847
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