联合作者(
Maria Li Lung Clinical Oncology Department, The Univerisity of Hong Kong, Hong Kong SAR
3 protocols
联合评审(
Agnieszka Pastula Umeå University Umeå
6 protocols

Andrea Puhar MIMS and Department of Molecular Biology, Umeå University
53 protocols

Anita Umesh Illumina
4 protocols

Benoit Chassaing Georgia State University
14 protocols

编委
HongLok Lung
  • Faculty, University of Hong Kong
研究方向
  • 癌症生物学
  • 已发表 protocol 1

Education

Ph.D. in Biochemistry, the Chinese University of Hong Kong, 1999

Current position

Assistant Professor, Clinical Oncology, the University of Hong Kong

My major research interests and projects: My current projects are mainly focused on the cancer genetics and the associated tumor microenvironment of nasopharyngeal carcinoma (NPC). We have previously identified some NPC tumor suppressor genes (TSGs) by using the functional complementation approach and the subsequent gene profiling and genotyping analyses. We are characterizing their tumor suppressive function and association with angiogenesis in NPC. Polymorphism analysis of some of our TSGs and their associations with NPC risk are my other major research interest. In addition, I am also interested to investigate whether the aggressive/metastatic phenotype of NPC cell lines is associated with tumor hypoxia

Publications (selected)

  1. Lung, H. L.,andLung, M. L. (2012). In vivo Matrigel Plug Angiogenesis Assay. Bio-Protocol 2(18).
  2. Lung, H. L., Cheung, A. K. L., Ko, J. M. Y., Cheng, Y. and Lung, M. L. (2012). Identification of tumor suppressor genes via cell fusion and chromosomal transfer. Tumor Suppressor Genes. InTech: Croatia: 53-78.
  3. Lung, H. L., Cheung, A. K., Ko, J. M., Cheng, Y., Stanbridge, E. J. and Lung, M. L. (2012). Deciphering the molecular genetic basis of NPC through functional approaches. Semin Cancer Biol 22(2): 87-95.
  4. Huang, Z., Cheng, Y., Chiu, P. M., Cheung, F. M., Nicholls, J. M., Kwong, D. L., Lee, A. W., Zabarovsky, E. R., Stanbridge, E. J., Lung, H. L.* and Lung, M. L.* (2012). Tumor suppressor Alpha B-crystallin (CRYAB) associates with the cadherin/catenin adherens junction and impairs NPC progression-associated properties. Oncogene 31(32): 3709-3720. (*co-corresponding authorship)
  5. Cheung, A. K., Ko, J. M., Lung, H. L., Chan, K. W., Stanbridge, E. J., Zabarovsky, E., Tokino, T., Kashima, L., Suzuki, T., Kwong, D. L., Chua, D., Tsao, S. W. and Lung, M. L. (2011). Cysteine-rich intestinal protein 2 (CRIP2) acts as a repressor of NF-kappaB-mediated proangiogenic cytokine transcription to suppress tumorigenesis and angiogenesis. Proc Natl Acad Sci U S A 108(20): 8390-8395.
  6. Lo, P. H.*, Lung, H. L.*, Cheung, A. K., Apte, S. S., Chan, K. W., Kwong, F. M., Ko, J. M., Cheng, Y., Law, S., Srivastava, G., Zabarovsky, E. R., Tsao, S. W., Tang, J. C., Stanbridge, E. J. and Lung, M. L. (2010). Extracellular protease ADAMTS9 suppresses esophageal and nasopharyngeal carcinoma tumor formation by inhibiting angiogenesis. Cancer Res 70(13): 5567-5576. (*co-first authorship)
  7. Lung, H. L., Cheung, A. K., Cheng, Y., Kwong, F. M., Lo, P. H., Law, E. W., Chua, D., Zabarovsky, E. R., Wang, N., Tsao, S. W., Stanbridge, E. J. and Lung, M. L. (2010). Functional characterization of THY1 as a tumor suppressor gene with antiinvasive activity in nasopharyngeal carcinoma. Int J Cancer 127(2): 304-312.
  8. Cheung, A. K., Lung, H. L., Ko, J. M., Cheng, Y., Stanbridge, E. J., Zabarovsky, E. R., Nicholls, J. M., Chua, D., Tsao, S. W., Guan, X. Y. and Lung, M. L. (2009). Chromosome 14 transfer and functional studies identify a candidate tumor suppressor gene, mirror image polydactyly 1, in nasopharyngeal carcinoma. Proc Natl Acad Sci U S A 106(34): 14478-14483.
  9. Cheung, A. K., Lung, H. L., Hung, S. C., Law, E. W., Cheng, Y., Yau, W. L., Bangarusamy, D. K., Miller, L. D., Liu, E. T., Shao, J. Y., Kou, C. W., Chua, D., Zabarovsky, E. R., Tsao, S. W., Stanbridge, E. J. and Lung, M. L. (2008). Functional analysis of a cell cycle-associated, tumor-suppressive gene, protein tyrosine phosphatase receptor type G, in nasopharyngeal carcinoma. Cancer Res 68(19): 8137-8145.
  10. Lung, H. L., Lo, P. H., Xie, D., Apte, S. S., Cheung, A. K., Cheng, Y., Law, E. W., Chua, D., Zeng, Y. X., Tsao, S. W., Stanbridge, E. J. and Lung, M. L. (2008). Characterization of a novel epigenetically-silenced, growth-suppressive gene, ADAMTS9, and its association with lymph node metastases in nasopharyngeal carcinoma. Int J Cancer 123(2): 401-408.
  11. Lung, H. L., Lo, C. C., Wong, C. C., Cheung, A. K., Cheong, K. F., Wong, N., Kwong, F. M., Chan, K. C., Law, E. W., Tsao, S. W., Chua, D., Sham, J. S., Cheng, Y., Stanbridge, E. J., Robertson, G. P. and Lung, M. L. (2008). Identification of tumor suppressive activity by irradiation microcell-mediated chromosome transfer and involvement of alpha B-crystallin in nasopharyngeal carcinoma. Int J Cancer 122(6): 1288-1296.
  12. Lung, H. L., Cheung, A. K., Xie, D., Cheng, Y., Kwong, F. M., Murakami, Y., Guan, X. Y., Sham, J. S., Chua, D., Protopopov, A. I., Zabarovsky, E. R., Tsao, S. W., Stanbridge, E. J. and Lung, M. L. (2006). TSLC1 is a tumor suppressor gene associated with metastasis in nasopharyngeal carcinoma. Cancer Res 66(19): 9385-9392.
  13. Lung, H. L., Bangarusamy, D. K., Xie, D., Cheung, A. K., Cheng, Y., Kumaran, M. K., Miller, L., Liu, E. T., Guan, X. Y., Sham, J. S., Fang, Y., Li, L., Wang, N., Protopopov, A. I., Zabarovsky, E. R., Tsao, S. W., Stanbridge, E. J. and Lung, M. L. (2005). THY1 is a candidate tumour suppressor gene with decreased expression in metastatic nasopharyngeal carcinoma. Oncogene 24(43): 6525-6532.
  14. Lung, H. L., Cheng, Y., Kumaran, M. K., Liu, E. T., Murakami, Y., Chan, C. Y., Yau, W. L., Ko, J. M., Stanbridge, E. J. and Lung, M. L. (2004). Fine mapping of the 11q22-23 tumor suppressive region and involvement of TSLC1 in nasopharyngeal carcinoma. Int J Cancer 112(4): 628-635.
已发表 protocol 1篇
In vivo Matrigel Plug Angiogenesis Assay
基质胶内血管生成实验

作者:Hong Lok Lung and Maria Li Lung日期:09/20/2012,浏览量:46187,Q&A: 4
The matrigel plug angiogenesis assay is a simple in vivo technique to detect the newly formed blood vessels in the transplanted gel plugs in nude mice. The matrigel matrix is derived from the engelbroth-holm-swarm (EHS) mouse sarcoma, and ...
参审 protocol 5篇
Isolating Brain Mitochondria by Differential Centrifugation
差速离心法分离脑线粒体
作者:Ignacio Amigo, Javier Traba and Carlos B. Rueda日期:05/20/2016,浏览量:13978,Q&A: 3
In addition to methods aimed at the study of mitochondrial function in-situ, a full understanding of mitochondrial function requires their purification from cells or tissues under specific physiological or pathological conditions. This ...
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Isolating Liver Mitochondria by Differential Centrifugation
差速离心法分离肝脏线粒体
作者:Ignacio Amigo, Javier Traba and Carlos B. Rueda日期:05/20/2016,浏览量:15302,Q&A: 0
In addition to methods aimed at the study of mitochondrial function in-situ, a full understanding of mitochondrial function requires their purification from cells or tissues under specific physiological or pathological conditions. This protocol ...
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主审 protocol 56篇
Modeling NOTCH1 driven T-cell Acute Lymphoblastic Leukemia in Mice
NOTCH1诱导小鼠T细胞急性淋巴细胞白血病模型的建立
作者:Agnieszka A. Wendorff and Adolfo A. Ferrando日期:05/20/2020,浏览量:2720,Q&A: 0
T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematological malignancy that arises from transformation of T-cell primed hematopoietic progenitors. Although T-ALL is a heterogenous and molecularly complex disease, more than 65% of ...
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Bone-in-culture Array to Model Bone Metastasis in ex vivo Condition
体外骨碎片培养列阵模拟骨转移
作者:Hai Wang and Xiang H.-F. Zhang日期:01/20/2020,浏览量:2351,Q&A: 0
Bone is the most frequently affected organ by metastases of breast cancer and prostate cancer. Our knowledge on bone metastasis is extremely limited due to the lack of potent and efficient experimental models. We developed the “Bone-In-Culture Array ...
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