Tumor-Targeting Peptides and Small Molecules as Anti-Cancer Agents to Overcome Drug Resistance

被引:14
|
作者
Sarafraz-Yazdi, Ehsan [1 ,2 ]
Pincus, Matthew R. [2 ,3 ]
Michl, Josef [2 ,4 ]
机构
[1] Suny Downstate Med Ctr, Dept Obstet & Gynecol, Div Gynecol Oncol, Brooklyn, NY 11203 USA
[2] Suny Downstate Med Ctr, Dept Pathol, Brooklyn, NY 11203 USA
[3] New York Harbor VA Med Ctr, Dept Pathol, Brooklyn, NY USA
[4] Suny Downstate Med Ctr, Dept Cell Biol, Brooklyn, NY 11203 USA
关键词
Anti-cancer peptides; drug resistance; small molecule inhibitors; targeted cancer therapy; SOMATOSTATIN RECEPTOR SCINTIGRAPHY; ANTI-CD20; MONOCLONAL-ANTIBODY; TYROSINE KINASE INHIBITORS; CHRONIC MYELOID-LEUKEMIA; HUMAN-BREAST CANCER; ACQUIRED-RESISTANCE; MULTIDRUG-RESISTANCE; SIGNALING PATHWAYS; ONCOGENIC RAS-P21; CHRONIC-PHASE;
D O I
10.2174/09298673113209990223
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Since the introduction of chemotherapy in cancer therapy, development of resistance to every new therapeutic has been the universal experience. The growing understanding of cancer genomics, cancer-associated signal transduction pathways, and key protein drivers of cancer has enabled cancer biologists and medicinal chemists to develop targeted molecules to interfere with these pathways to tackle drug resistant cancers. However, to the dismay of oncologists, the clinical use of many of these tools has once again brought to the forefront the inevitable challenge of drug resistance. It is now understood that cancer resistance to different therapies involves multiple challenges that encompass the cancer cell itself as well as host physiology. This review presents small molecule inhibitors and peptides as two therapeutic approaches in anti-cancer drug development. Resistance to selected samples of these novel therapies is described in the context of cell autonomous resistance, the contributions of the tumor microenvironment, and germ line factors. For each approach, advantages and disadvantages are discussed on how to better overcome the inevitable challenge of resistance in cancer treatment.
引用
收藏
页码:1618 / 1630
页数:13
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