L
Lance D. Miller
Researcher at Wake Forest University
Publications - 208
Citations - 16169
Lance D. Miller is an academic researcher from Wake Forest University. The author has contributed to research in topics: Cancer & Breast cancer. The author has an hindex of 58, co-authored 195 publications receiving 14459 citations. Previous affiliations of Lance D. Miller include University of Texas MD Anderson Cancer Center & East Carolina University.
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Journal ArticleDOI
Frequent decreased expression of candidate tumor suppressor gene, DEC1, and its anchorage-independent growth properties and impact on global gene expression in esophageal carcinoma.
Alfred Chi Chung Leung,Victor Chun Lam Wong,Li Chun Yang,Pui Ling Chan,Yataro Daigo,Yusuke Nakamura,Robert Z. Qi,Lance D. Miller,Edison T. Liu,Li-Dong Wang,Ji-Lin Li,Simon Law,Sai Wah Tsao,Maria Li Lung +13 more
TL;DR: The studies show that DEC1 is involved in esophageal cancer development and help elucidate its functional role in tumor development and show statistically significant differences in colony numbers with the vector‐alone controls.
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Prognostic value of the hDMP1-ARF-Hdm2-p53 pathway in breast cancer
Dejan Maglic,Sinan Zhu,Elizabeth A. Fry,Pankaj Taneja,Fumitake Kai,Robert D. Kendig,Takayuki Sugiyama,Lance D. Miller,Mark C. Willingham,Kazushi Inoue +9 more
TL;DR: Human breast epithelial cells/cancer cells with wild-type p53 were sensitive to growth inhibition by activated Dmp1:ER while those that delete p14ARF or p53, and/or Hdm2 amplification showed partial or nearly complete resistance, indicating that p53 is a critical target for hDMP1 to exhibit its biological activity.
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Activin A Promotes Regulatory T-cell-Mediated Immunosuppression in Irradiated Breast Cancer.
Mara De Martino,Camille Daviaud,Julie M. Diamond,Julie M. Diamond,Jeffrey Kraynak,Amandine Alard,Silvia C. Formenti,Lance D. Miller,Sandra Demaria,Claire Vanpouille-Box +9 more
TL;DR: Light is shed on an immune escape mechanism driven by activin A and dual targeting of activation A and TGFβ may be required to optimally unleash radiation-induced antitumor immunity against breast cancer, and retrospective analysis of a public dataset of patients with breast cancer revealed a positive correlation betweenactivin A gene expression and Treg abundance.
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Identifying gene expression changes in breast cancer that distinguish early and late relapse among uncured patients
TL;DR: The results show that the proposed statistic provides a more powerful basis for gene selection than the classical Cox model-based statistic and many of the genes identified here as associated with the speed of disease recurrence have known roles in tumorigenesis.
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Monochromosome transfer and microarray analysis identify a critical tumor-suppressive region mapping to chromosome 13q14 and THSD1 in esophageal carcinoma.
Josephine Mun Yee Ko,Pui Ling Chan,Wing Lung Yau,Ho Kin Chan,King Chi Chan,Zhuo You Yu,Fung Mei Kwong,Lance D. Miller,Edison T. Liu,Li Chun Yang,Paulisally Hau Yi Lo,Eric J. Stanbridge,Johnny Cheuk On Tang,Gopesh Srivastava,Sai Wah Tsao,Simon Law,Maria Li Lung +16 more
TL;DR: Results suggest that the tumor-suppressing effect is not attributed to RB1, but instead likely involves thrombospondin type I domain-containing 1 (THSD1), a novel candidate TSG mapping to 13q14.