Human Ductal Carcinoma In Situ: Advances and Future Perspectives

被引:3
作者
Behbod, Fariba [1 ]
Chen, Jennifer H. [2 ]
Thompson, Alastair [3 ]
机构
[1] Univ Kansas, Med Ctr, Dept Pathol & Lab Med, MS 3045, Kansas City, KS 66160 USA
[2] Baylor Coll Med, Michael E DeBakey Dept Surg, Houston, TX 77030 USA
[3] Baylor Coll Med, Lester & Sue Smith Breast Ctr, Dan L Duncan Comprehens Canc Ctr, Sect Breast Surg, Houston, TX 77030 USA
关键词
COMPARATIVE GENOMIC HYBRIDIZATION; INVASIVE BREAST-CANCER; MYOEPITHELIAL CELL; RISK-FACTORS; TUMOR-CELLS; PHASE-III; PROGRESSION; EXPRESSION; CAVEOLIN-1; GRADE;
D O I
10.1101/cshperspect.a041319
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Due to widespread adoption of screening mammography, there has been a significant increase in new diagnoses of ductal carcinoma in situ (DCIS). However, DCIS outcomes remain unclear. A large fraction of human DCIS (>50%) may not need the multimodality treatment options currently offered to all DCIS patients. More importantly, while we may be overtreating many, we cannot identify those most at risk of invasion or metastasis following a DCIS diagnosis. This review summarizes the studies that have furthered our understanding of DCIS pathology and mechanisms of invasive progression by using advanced technologies including spatial genomics, transcriptomics, and multiplex proteomics. This review also highlights a need for rethinking DCIS with a more focused view on epithelial states and programs and their cross talk with the microenvironment.
引用
收藏
页数:22
相关论文
共 85 条
[1]   A Molecular Portrait of High-Grade Ductal Carcinoma In Situ [J].
Abba, Martin C. ;
Gong, Ting ;
Lu, Yue ;
Lee, Jaeho ;
Zhong, Yi ;
Lacunza, Ezequiel ;
Butti, Matias ;
Takata, Yoko ;
Gaddis, Sally ;
Shen, Jianjun ;
Estecio, Marcos R. ;
Sahin, Aysegul A. ;
Aldaz, C. Marcelo .
CANCER RESEARCH, 2015, 75 (18) :3980-3990
[2]   Chromosomal copy number alterations for associations of ductal carcinoma in situ with invasive breast cancer [J].
Afghahi, Anosheh ;
Forgo, Erna ;
Mitani, Aya A. ;
Desai, Manisha ;
Varma, Sushama ;
Seto, Tina ;
Rigdon, Joseph ;
Jensen, Kristin C. ;
Troxell, Megan L. ;
Gomez, Scarlett Lin ;
Das, Amar K. ;
Beck, Andrew H. ;
Kurian, Allison W. ;
West, Robert B. .
BREAST CANCER RESEARCH, 2015, 17
[3]   Molecular characterization of the tumor microenvironment in breast cancer [J].
Allinen, M ;
Beroukhim, R ;
Cai, L ;
Brennan, C ;
Lahti-Domenici, J ;
Huang, HY ;
Porter, D ;
Hu, M ;
Chin, L ;
Richardson, A ;
Schnitt, S ;
Sellers, WR ;
Polyak, K .
CANCER CELL, 2004, 6 (01) :17-32
[4]   Ductal carcinoma in situ and the emergence of diversity during breast cancer evolution [J].
Allred, D. Craig ;
Wu, Yun ;
Mao, Sufeng ;
Nagtegaal, Iris D. ;
Lee, Sangjun ;
Perou, Charles M. ;
Mohsin, Syed K. ;
O'Connell, Peter ;
Tsimelzon, Anna ;
Medina, Dan .
CLINICAL CANCER RESEARCH, 2008, 14 (02) :370-378
[5]  
Barcellos-Hoff MH, 2000, CANCER RES, V60, P1254
[6]   The reverse Warburg effect Glycolysis inhibitors prevent the tumor promoting effects of caveolin-1 deficient cancer associated fibroblasts [J].
Bonuccelli, Gloria ;
Whitaker-Menezes, Diana ;
Castello-Cros, Remedios ;
Pavlides, Stephanos ;
Pestell, Richard G. ;
Fatatis, Alessandro ;
Witkiewicz, Agnieszka K. ;
Vander Heiden, Matthew G. ;
Migneco, Gemma ;
Chiavarina, Barbara ;
Frank, Philippe G. ;
Capozza, Franco ;
Flomenberg, Neal ;
Martinez-Outschoorn, Ubaldo E. ;
Sotgia, Federica ;
Lisanti, Michael P. .
CELL CYCLE, 2010, 9 (10) :1960-1971
[7]   A Biological Signature for Breast Ductal Carcinoma In Situ to Predict Radiotherapy Benefit and Assess Recurrence Risk [J].
Bremer, Troy ;
Whitworth, Pat W. ;
Patel, Rakesh ;
Savala, Jess ;
Barry, Todd ;
Lyle, Stephen ;
Leesman, Glen ;
Linke, Steven P. ;
Jirstrom, Karin ;
Zhou, Wenjing ;
Amini, Rose-Marie ;
Warnberg, Fredrik .
CLINICAL CANCER RESEARCH, 2018, 24 (23) :5895-5901
[8]  
Buerger H, 1999, J PATHOL, V187, P396, DOI 10.1002/(SICI)1096-9896(199903)187:4<396::AID-PATH286>3.0.CO
[9]  
2-L
[10]   Multiclonal Invasion in Breast Tumors Identified by Topographic Single Cell Sequencing [J].
Casasent, Anna K. ;
Schalck, Aislyn ;
Gao, Ruli ;
Sei, Emi ;
Long, Annalyssa ;
Pangburn, William ;
Casasent, Tod ;
Meric-Bernstam, Funda ;
Edgerton, Mary E. ;
Navin, Nicholas E. .
CELL, 2018, 172 (1-2) :205-+