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Journal of Thoracic Oncology:
doi: 10.1097/JTO.0b013e3181ce3afd
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TGF-β Signaling and the Role of Inhibitory Smads in Non-small Cell Lung Cancer

Jeon, Hyo-Sung PhD*; Jen, Jin MD, PhD†

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*Department of Biochemistry and Cell Biology, School of Medicine, Kyungpook National University, Daegu, Republic of Korea; and †Department of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, Minnesota.

Disclosure: The authors declare no conflict of interest.

Address for correspondence: Jin Jen, MD, PhD, Department of Pulmonary and Critical Care Medicine, Mayo Clinic, Rochester, MN 55905. E-mail: Jen.Jin@mayo.edu, or Hyo-Sung Jeon, PhD, Department of Biochemistry and Cell Biology, School of Medicine, Kyungpook National University, Daegu 702-422, Republic of Korea. E-mail: jeonh@knu.ac.kr

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Abstract

The signaling pathway mediated by transforming growth factor-β (TGF-β) participates in various biologic processes, including cell growth, differentiation, angiogenesis, apoptosis, and extracellular matrix remodeling. In the context of cancer, TGF-β signaling can inhibit tumor growth in early-stage tumors. However, in late-stage tumors, the very same pathway promotes tumor invasiveness and metastasis. This paradoxical effect is mediated through similar to mothers against decapentaplegic or Smad protein dependent and independent mechanisms and provides an opportunity for targeted cancer therapy. This review summarizes the molecular process of TGF-β signaling and the changes in inhibitory Smads that contribute to lung cancer progression. We also present current approaches for rational therapies that target the TGF-β signaling pathway in cancer.

Transforming growth factor (TGF-β) belongs to a superfamily of structurally related polypeptides that also includes TGF-β2, TGF-β3, Activins, Nodals, and bone morphogenetic (BMP) proteins.1,2 TGF-β receptor I (TGF-β RI) is recruited to the complex by ligand binding to a heteromeric complex of type I and type II (TGF-β RII) receptors, which are serine/threonine kinase transmembrane proteins. This results in the activation of TGF-β RII kinase domain in the cytoplasm and then phosphorylates receptor-regulated Smad proteins (R-Smad), Smad2 and Smad3. Activated phospho-Smad2 and 3 bind with common mediated Smad (co-Smad), Smad4, and translocate to the nucleus, which in turn regulates transcription in a diverse array of genes (Figure 1).3 TGF-β signaling is subjected to negative feedback by two inhibitory Smads (I-Smad), Smad6 and Smad7. Both I-Smads can interfere the phosphorylation of Smad2/3 by interaction with TGF-β RI.4,5 The termination of TGF-β signaling can also be achieved through ubiquitination of TGF-β RI and I-Smads by ubiquitin ligases Smad ubiquitin regulatory factors 1 and 2 (Smurf1 and Smurf2), which promote polyubiquitination followed by lysosomal-mediated degradation (Figure 1).6 In addition to Smads mediated signaling, TGF-β can also activate Smad-independent pathways in different cell contexts.7,8

Figure 1
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TGF-β and Cancer

Alterations in TGF-β signaling are linked to a variety of human diseases, including cancer and inflammation. Disruption of TGF-β homeostasis occurs in several human cancers.9,10 Data from both experimental model systems and studies of human cancers clearly show that not only the ligand itself but also its downstream elements, including its receptors and its primary cytoplasmic signal transducers, the Smad proteins, are important in suppressing primary tumorigenesis in many tissue types.11 However, many human cancers, including lung cancer, often overexpress TGF-β. Furthermore, TGF-β enhances the invasiveness and metastatic potential in certain late-stage tumors.12 The role of TGF-β in cancer progression and metastasis is generally accompanied by decreased or altered TGF-β responsiveness and increased expression or activation of the TGF-β ligand.12 In the immunocytochemical analysis, localization of secreted TGF-β is found at the advancing edges of primary tumors and in lymph node metastases of human mammary carcinoma.13 High levels of TGF-β were also detected in the serum of patients with lung cancer and colorectal carcinomas compared with nondiseased individuals, and TGF-β level in serum is deceased to normal range after surgical resection of the tumor in colorectal cancer.14,15 This suggests that both autocrine and paracrine effects of TGF-β contribute to promote tumor progression.

Although most lung cancer cells secrete TGF-β, the malignant transformation in lung cancer results in a loss of the tumor suppressor effects of TGF-β. Loss of the TGF-β response, which results in lost of inhibitory effect of TGF-β on proliferation, has been associated with tumor development and/or tumor progression in several cancers.16,17 Reduced expression and inactivation of TGF-β receptors were associated with loss of sensitivity with antiproliferative effects of TGF-β in carcinogenesis.11 In lung cancer, overexpression of TGF-β is associated with better prognosis in 5-year patient survival.18 TGF-β1 level in serum was elevated after radiotherapy in lung cancer, and the risk of radiation-induced lung injury is associated with TGF-β1 single nucleotide polymorphism.19,20

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I-Smads and TGF-β Signaling

The feedback mechanisms that regulate TGF-β signaling play a central role in cellular homeostasis mediated by TGF-β (Figure 1). The transcriptional activation of I-Smads is induced by TGF-β and other signaling pathways such as EGF, interferon gamma, and interleukin 1β.21–23 I-Smads (Smad6 and Smad7) regulate TGF-β function by interfering with receptor-mediated phosphorylation of Smad2/3.5,24 Generally, Smad6 is thought to repress BMP signaling, whereas Smad7 represses the TGF-β signaling pathway.21 However, both proteins can regulate the TGF-β signaling pathway through negative regulation in lung epithelial cells.25 In lung cancer, Smad6 is overexpressed in a portion of the tumors, and high expression of Smad6 is associated with poor survival in patients with non-small cell lung cancer.26 Knockdown of Smad6 in overexpressed lung cancer cells induced apoptosis and growth arrest at the G1 phase, which contributed to the reestablishment of TGF-β homeostasis in lung cancer cells by reactivating the TGF-β signal pathway.26 Similarly, overexpression of Smad7 causes malignant conversion in multistage cancer models by cooperating with oncogenic Ras and enhances tumorigenicity in pancreatic cancer.27,28 Furthermore, stable expression of Smad7 impairs bone metastasis in human melanoma cells and lung and liver metastasis in JygMC(A) breast cancer cells.29,30 These studies indicate that I-Smads play a critical role in tumorigenesis by regulating TGF-β homeostasis in normal and cancer cells. Therapies targeting I-Smads could potentially help re-establish TGF-β mediated growth inhibition in tumors and enhance patient survival.

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Development of TGF-β Signaling Inhibitors for Cancer Treatment

TGF-β suppresses early epithelial cancers by TGF-β-mediated growth inhibition. As premalignant lesions progress, TGF-β signaling contributes to tumor progression by inducing epithelial-to-mesenchymal transition (EMT), thereby promoting the conversion of early epithelial tumors to invasive, metastatic tumors.31 Many inhibitors of TGF-β signaling target the EMT process. For example, the small molecule ATP competitive compounds SB-505124 and SB-431542 have been developed as inhibitors against the enzymatic activity of the TGF-β RI type receptor called activin receptor-like kinase ALK5.32–34 These drugs have been shown to inhibit TGF-β-induced cell migration and invasiveness in glioma or EMT in vitro.

In addition to small molecules, antibodies have been developed. The TGF-β antibody inhibits phosphatidylinositol-3 kinase (PI3K)/AKT activity in mammary cancer cells by neutralizing TGF-β protein and suppresses the growth of renal cell carcinoma overexpressing TGF-β.35,36 Antisense oligonucleotides have been developed to directly target TGF-β2 mRNA. Recently, targeted TGF-β2 suppression using AP 12009 has emerged as a promising novel approach for treating malignant gliomas and other highly aggressive TGF-β2-overexpressing tumors.37 Little studies have been done targeting TGF-β signaling pathway in lung cancer. However, our recent study suggests that Smad6 protein contributes to lung cancer survival and targeting Smad6 may serve as an effective means to reduce tumor growth and improve patient outcome.26

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CONCLUSION

TGF-β signaling contributes to diverse cellular processes and plays a critical role in lung cancer growth and progression. TGF-β generally serves as a negative growth regulator in normal cells and early stage tumor development, but it promotes tumor invasiveness and metastases by inducing EMT and neoangiogenesis. Current strategies focus on developing effective therapies that target mainly the tumor-promoting activities of TGF-β signaling. However, the complex nature and dual effects of TGF-β signaling in cancer must be considered together to be effective in clinical trials for cancer therapy. This requires combinational therapies that seek to interfere with both TGF-β/Smads dependent- and independent-signaling processes.

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ACKNOWLEDGMENTS

Supported in part by a grant from the national R&D Program for Cancer Control Ministry of Health & Welfare, Republic of Korea (0720550-2) and the Brain Korea 21 Project (to H.S.J.) and by Research Funds from the Mayo Cancer Center and the Mayo Center for Individualized Medicine (to J.J.).

The authors thank Ms. Stacy Johnson for manuscript editing.

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Keywords:

TGF-β signaling; Smads; Non-small cell lung cancer survival; Target-based therapy

© 2010International Association for the Study of Lung Cancer

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