TY - JOUR
T1 - Prognostic significance of NPM-ALK fusion transcript overexpression in ALK-positive anaplastic large-cell lymphoma
AU - Li, Chunmei
AU - Takino, Hisashi
AU - Eimoto, Tadaaki
AU - Ishida, Takashi
AU - Inagaki, Atsushi
AU - Ueda, Ryuzo
AU - Suzuki, Ritsuro
AU - Yoshino, Tadashi
AU - Nakagawa, Atsuko
AU - Nakamura, Shigeo
AU - Inagaki, Hiroshi
N1 - Funding Information:
This work was supported in part by a Grant-in-Aid from the Ministry of Education, Science, Sports, and Culture of Japan to HI and CL. A Postdoctoral Fellowship for Foreign Researchers to CL from the Japan Society for the Promotion of Science (JSPS) is gratefully acknowledged.
PY - 2007/6
Y1 - 2007/6
N2 - In anaplastic large-cell lymphomas positive for anaplastic lymphoma kinase (ALK) protein, the ALK gene is most commonly fused to the NPM gene, and less commonly to TPM3, TFG, ATIC, and other rare genes. Although this lymphoma is generally associated with a favorable clinical outcome, 25% of the patients die of the disease within 5 years. In this study, we developed three assays, all of which can be used with archival formalin-fixed, paraffin-embedded tissues: (1) a sensitive reverse transcription-polymerase chain reaction (RT-PCR) assay for various X-ALK fusion genes, (2) a 5′ rapid amplification of cDNA ends (RACE) assay to identify unknown fusion partners, and (3) a real-time RT-PCR assay to quantify the amount of the NPM-ALK fusion transcript. In 26 cases of ALK+ anaplastic large-cell lymphoma, the RT-PCR assay showed that the ALK was fused to NPM in 21 cases, to TPM3 in three, and to TFG in one. The 5′ RACE assay detected ATIC-ALK fusion in the remaining case. The real-time quantitative RT-PCR assay showed that the NPM-ALK transcript was over expressed in four of 20 quantifiable cases. Patients with NPM-ALK overexpression showed a significantly unfavorable overall survival compared with those with a low expression of this transcript. The RT-PCR and 5′ RACE assays developed here may be useful for identification of known and unknown gene partners fused to the ALK gene. Overexpression of the NPM-ALK fusion transcript may be associated with a poor prognosis of the patients with ALK+ anaplastic large-cell lymphomas.
AB - In anaplastic large-cell lymphomas positive for anaplastic lymphoma kinase (ALK) protein, the ALK gene is most commonly fused to the NPM gene, and less commonly to TPM3, TFG, ATIC, and other rare genes. Although this lymphoma is generally associated with a favorable clinical outcome, 25% of the patients die of the disease within 5 years. In this study, we developed three assays, all of which can be used with archival formalin-fixed, paraffin-embedded tissues: (1) a sensitive reverse transcription-polymerase chain reaction (RT-PCR) assay for various X-ALK fusion genes, (2) a 5′ rapid amplification of cDNA ends (RACE) assay to identify unknown fusion partners, and (3) a real-time RT-PCR assay to quantify the amount of the NPM-ALK fusion transcript. In 26 cases of ALK+ anaplastic large-cell lymphoma, the RT-PCR assay showed that the ALK was fused to NPM in 21 cases, to TPM3 in three, and to TFG in one. The 5′ RACE assay detected ATIC-ALK fusion in the remaining case. The real-time quantitative RT-PCR assay showed that the NPM-ALK transcript was over expressed in four of 20 quantifiable cases. Patients with NPM-ALK overexpression showed a significantly unfavorable overall survival compared with those with a low expression of this transcript. The RT-PCR and 5′ RACE assays developed here may be useful for identification of known and unknown gene partners fused to the ALK gene. Overexpression of the NPM-ALK fusion transcript may be associated with a poor prognosis of the patients with ALK+ anaplastic large-cell lymphomas.
KW - Anaplastic large-cell lymphoma
KW - Clinicopathological study
KW - NPM-ALK fusion transcript
KW - RACE
KW - RT-PCR
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U2 - 10.1038/modpathol.3800781
DO - 10.1038/modpathol.3800781
M3 - Article
C2 - 17464320
AN - SCOPUS:34249036194
SN - 0893-3952
VL - 20
SP - 648
EP - 655
JO - Modern Pathology
JF - Modern Pathology
IS - 6
ER -