1.Combined Modality Therapy for Locally Advanced Non-Small Cell Lung Cancer.
L Chinsoo CHO ; J Michael DIMAIO ; Randall HUGHES ; Phuc NGUYEN ; Paula ANDERSON ; Hak CHOY
Cancer Research and Treatment 2003;35(5):373-382
The majority of non-small cell lung cancer patients present with locally advanced disease that may not be resectable. A single modality treatment such as thoracic radiotherapy often results in an inferior outcome when compared to combined modality treatment. Various combinations of radiotherapy, chemotherapy, and surgery have been tested in patients with locally advanced non-small-celllung cancer with promising results. The favorable results of the combined modality treatment are accompanied by a corresponding increase in treatment related morbidity. In this article, the results of the application of combined modality treatments in the management of locally advanced non-small cell lung cancer are reviewed.
Carcinoma, Non-Small-Cell Lung*
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Combined Modality Therapy*
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Drug Therapy
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Humans
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Radiotherapy
2.Loss of podocalyxin causes a novel syndromic type of congenital nephrotic syndrome.
Hee Gyung KANG ; Moses LEE ; Kyoung Boon LEE ; Michael HUGHES ; Bo Sang KWON ; Sangmoon LEE ; Kelly M MCNAGNY ; Yo Han AHN ; Jung Min KO ; Il Soo HA ; Murim CHOI ; Hae Il CHEONG
Experimental & Molecular Medicine 2017;49(12):e414-
Many cellular structures directly imply specific biological functions. For example, normal slit diaphragm structures that extend from podocyte foot processes ensure the filtering function of renal glomeruli. These slits are covered by a number of surface proteins, such as nephrin, podocin, podocalyxin and CD2AP. Here we report a human patient presenting with congenital nephrotic syndrome, omphalocele and microcoria due to two loss-of-function mutations in PODXL, which encodes podocalyxin, inherited from each parent. This set of symptoms strikingly mimics previously reported mouse Podxl(−/−) embryos, emphasizing the essential function of PODXL in mammalian kidney development and highlighting this patient as a human PODXL-null model. The results underscore the utility of current genomics approaches to provide insights into the genetic mechanisms of human disease traits through molecular diagnosis.