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Items: 1 to 20 of 108

1.
Amphiregulin regulates the activation of ERK and Akt through epidermal growth factor receptor and HER3 signals involved in the progression of pancreatic cancer
Fusanori Yotsumoto, Tatsuya Fukami, Hiroshi Yagi, Akihiro Funakoshi, Toshiyuki Yoshizato, Masahide Kuroki, Shingo Miyamoto
Cancer Sci. 2010 Nov; 101(11): 2351–2360. Published online 2010 Jul 7. doi: 10.1111/j.1349-7006.2010.01671.x
PMCID:
PMC11158290
AbstractArticlePDF–769K
2.
Clinical significance of pretreatment serum amphiregulin and transforming growth factor‐α, and an epidermal growth factor receptor somatic mutation in patients with advanced non‐squamous, non‐small cell lung cancer
Katsuhiro Masago, Shiro Fujita, Yukimasa Hatachi, Akiko Fukuhara, Keiichiro Sakuma, Masataka Ichikawa, Yung Haku Kim, Tadashi Mio, Michiaki Mishima
Cancer Sci. 2008 Nov; 99(11): 2295–2301. Published online 2008 Sep 22. doi: 10.1111/j.1349-7006.2008.00931.x
PMCID:
PMC11158209
AbstractArticlePDF–175K
3.
Mitochondrial dysfunction-induced amphiregulin upregulation mediates chemo-resistance and cell migration in HepG2 cells
C.-J. Chang, P.-H. Yin, D.-M. Yang, C.-H. Wang, W.-Y. Hung, C.-W. Chi, Y.-H. Wei, H.-C. Lee
Cell Mol Life Sci. 2009 May; 66(10): 1755–1765. Published online 2009 Apr 2. doi: 10.1007/s00018-009-8767-5
PMCID:
PMC11115798
AbstractArticlePDF–2.4M
4.
CD133 Stimulates Cell Proliferation via the Upregulation of Amphiregulin in Melanoma
Cynthia M Simbulan-Rosenthal, Nusrat Islam, Yogameenakshi Haribabu, Ryyan Alobaidi, Azadeh Shalamzari, Garrett Graham, Li-Wei Kuo, Peter Sykora, Dean S Rosenthal
Cells. 2024 May; 13(9): 777. Published online 2024 May 2. doi: 10.3390/cells13090777
PMCID:
PMC11083289
AbstractArticlePDF–13M
5.
Mucosal-associated invariant T cells promote ductular reaction through amphiregulin in biliary atresia
Man-Huan Xiao, Sihan Wu, Peishi Liang, Dong Ma, Jiang Zhang, Huadong Chen, Zhihai Zhong, Juncheng Liu, Hong Jiang, Xuyang Feng, Zhenhua Luo
eBioMedicine. 2024 May; 103: 105138. Published online 2024 Apr 27. doi: 10.1016/j.ebiom.2024.105138
PMCID:
PMC11077624
AbstractArticlePDF–3.8M
6.
EGF, TGF-α and Amphiregulin Differently Regulate Endometrium-Derived Mesenchymal Stromal/Stem Cells
Rimma Sergeevna Kamentseva, Marianna Viktorovna Kharchenko, Gulnara Vladikovna Gabdrahmanova, Michael Alexandrovich Kotov, Vera Vladislavovna Kosheverova, Elena Sergeevna Kornilova
Int J Mol Sci. 2023 Sep; 24(17): 13408. Published online 2023 Aug 29. doi: 10.3390/ijms241713408
PMCID:
PMC10487484
AbstractArticlePDF–26M
7.
miR-33a-3p regulates METTL3-mediated AREG stability and alters EMT to inhibit pancreatic cancer invasion and metastasis
Xiaowen Su, Tiantian Lai, Yue Tao, Yong Zhang, Changyong Zhao, Junjing Zhou, Enhong Chen, Maoqun Zhu, Shuo Zhang, Bei Wang, Yong Mao, Hao Hu
Sci Rep. 2023; 13: 13587. Published online 2023 Aug 21. doi: 10.1038/s41598-023-39506-7
PMCID:
PMC10442451
AbstractArticlePDF–10M
8.
Role of MR1-driven signals and amphiregulin on the recruitment and repair function of MAIT cells during skin wound healing
Anastasia du Halgouet, Aurélie Darbois, Mansour Alkobtawi, Martin Mestdagh, Aurélia Alphonse, Virginie Premel, Thomas Yvorra, Ludovic Colombeau, Raphaël Rodriguez, Dietmar Zaiss, Yara El Morr, Hélène Bugaut, François Legoux, Laetitia Perrin, Selim Aractingi, Rachel Golub, Olivier Lantz, Marion Salou
Immunity. 2023 Jan 10; 56(1): 78–92.e6. doi: 10.1016/j.immuni.2022.12.004
PMCID:
PMC9839364
AbstractArticle
9.
High cutaneous amphiregulin expression predicts fatal acute graft‐versus‐host disease
Brittney Schultz, Daniel D. Miller, Todd DeFor, Bruce R. Blazar, Angela Panoskaltsis‐Mortari, Brian C. Betts, Margaret L. MacMillan, Daniel J. Weisdorf, Shernan G. Holtan
J Cutan Pathol. 2022 Jun; 49(6): 532–535. Published online 2022 Mar 13. doi: 10.1111/cup.14218
PMCID:
PMC9311189
AbstractArticlePDF–942K
10.
Loss of Amphiregulin drives inflammation and endothelial apoptosis in pulmonary hypertension
Jonathan Florentin, Jingsi Zhao, Yi-Yin Tai, Wei Sun, Lee L Ohayon, Scott P O’Neil, Anagha Arunkumar, Xinyi Zhang, Jianhui Zhu, Yassmin Al Aaraj, Annie Watson, John Sembrat, Mauricio Rojas, Stephen Y Chan, Partha Dutta
Life Sci Alliance. 2022 Nov; 5(11): e202101264. Published online 2022 Jun 22. doi: 10.26508/lsa.202101264
PMCID:
PMC9218345
AbstractArticlePDF–2.4M
11.
A protein interaction landscape of breast cancer
Minkyu Kim, Jisoo Park, Mehdi Bouhaddou, Kyumin Kim, Ajda Rojc, Maya Modak, Margaret Soucheray, Michael J. McGregor, Patrick O’Leary, Denise Wolf, Erica Stevenson, Tzeh Keong Foo, Dominique Mitchell, Kari A. Herrington, Denise P. Muñoz, Beril Tutuncuoglu, Kuei-Ho Chen, Fan Zheng, Jason F. Kreisberg, Morgan E. Diolaiti, John D. Gordan, Jean-Philippe Coppé, Danielle L. Swaney, Bing Xia, Laura van ’t Veer, Alan Ashworth, Trey Ideker, Nevan Krogan
Science. Author manuscript; available in PMC 2022 Apr 26.
Published in final edited form as: Science. 2021 Oct; 374(6563): eabf3066. Published online 2021 Oct 1. doi: 10.1126/science.abf3066
PMCID:
PMC9040556
AbstractArticlePDF–2.2M
12.
Amphiregulin can predict treatment resistance to palliative first-line cetuximab plus FOLFIRI chemotherapy in patients with RAS wild-type metastatic colorectal cancer
Sang-A Kim, Hyejoo Park, Kui-Jin Kim, Ji-Won Kim, Ji Hea Sung, Milang Nam, Ju Hyun Lee, Eun Hee Jung, Koung Jin Suh, Ji Yun Lee, Se Hyun Kim, Jeong-Ok Lee, Jin Won Kim, Yu Jung Kim, Jee Hyun Kim, Soo-Mee Bang, Jong Seok Lee, Keun-Wook Lee
Sci Rep. 2021; 11: 23803. Published online 2021 Dec 10. doi: 10.1038/s41598-021-03197-9
PMCID:
PMC8664812
AbstractArticlePDF–3.4M
13.
Microglial-stimulation of glioma invasion involves the EGFR ligand amphiregulin
Salvatore J. Coniglio, Jeffrey E. Segall
PLoS One. 2021; 16(11): e0260252. Published online 2021 Nov 29. doi: 10.1371/journal.pone.0260252
PMCID:
PMC8629255
AbstractArticlePDF–1.2M
14.
The combined detection of Amphiregulin, Cyclin A1 and DDX20/Gemin3 expression predicts aggressive forms of oral squamous cell carcinoma
Ekaterina Bourova-Flin, Samira Derakhshan, Afsaneh Goudarzi, Tao Wang, Anne-Laure Vitte, Florent Chuffart, Saadi Khochbin, Sophie Rousseaux, Pouyan Aminishakib
Br J Cancer. 2021 Oct 12; 125(8): 1122–1134. Published online 2021 Jul 21. doi: 10.1038/s41416-021-01491-x
PMCID:
PMC8505643
AbstractArticlePDF–4.2M
15.
Expression of Amphiregulin in Enchondromas and Central Chondrosarcomas
Daniele Moraes Losada, André Luiz da Cruz Ribeiro, Francisco Fontes Cintra, Guilherme Rossi Assis de Mendonça, Maurício Etchebehere, Eliane Maria Ingrid Amstalden
Clinics (Sao Paulo) 2021; 76: e2914. Published online 2021 Aug 16. doi: 10.6061/clinics/2021/e2914
Correction in:
Clinics (Sao Paulo). 2021; 76: e2914err.
PMCID:
PMC8366900
AbstractArticlePDF–1.4M
16.
Dual Proteome-scale Networks Reveal Cell-specific Remodeling of the Human Interactome
Edward L. Huttlin, Raphael J. Bruckner, Jose Navarrete-Perea, Joe R. Cannon, Kurt Baltier, Fana Gebreab, Melanie P. Gygi, Alexandra Thornock, Gabriela Zarraga, Stanley Tam, John Szpyt, Brandon M. Gassaway, Alexandra Panov, Hannah Parzen, Sipei Fu, Arvene Golbazi, Eila Maenpaa, Keegan Stricker, Sanjukta Guha Thakurta, Tian Zhang, Ramin Rad, Joshua Pan, David P. Nusinow, Joao A. Paulo, Devin K. Schweppe, Laura Pontano Vaites, J. Wade Harper, Steven P. Gygi
Cell. Author manuscript; available in PMC 2022 May 27.
Published in final edited form as: Cell. 2021 May 27; 184(11): 3022–3040.e28. Published online 2021 May 6. doi: 10.1016/j.cell.2021.04.011
PMCID:
PMC8165030
AbstractArticlePDF–2.2M
17.
Targeting autocrine amphiregulin robustly and reproducibly inhibits ovarian cancer in a syngeneic model: roles for wildtype p53
Moshit Lindzen, Soma Ghosh, Ashish Noronha, Diana Drago, Nishanth Belugali Nataraj, Orith Leitner, Silvia Carvalho, Einav Zmora, Stav Sapoznik, Keren Bahar Shany, Keren Levanon, Dan Aderka, Belinda Sánchez Ramírez, Maik Dahlhoff, Iain McNeish, Yosef Yarden
Oncogene. 2021; 40(21): 3665–3679. Published online 2021 Apr 30. doi: 10.1038/s41388-021-01784-8
PMCID:
PMC8154589
AbstractArticlePDF–3.4M
18.
Dysregulation of Amphiregulin stimulates the pathogenesis of cystic lymphangioma
Naofumi Yoshida, Seiji Yamamoto, Takeru Hamashima, Noriko Okuno, Naruho Okita, Shinjiro Horikawa, Masao Hayashi, Thanh Chung Dang, Quang Linh Nguyen, Koichi Nishiyama, Teruhiko Makino, Yoko Ishii, Kei Tomihara, Tadamichi Shimizu, Masabumi Shibuya, Makoto Noguchi, Masakiyo Sasahara
Proc Natl Acad Sci U S A. 2021 May 11; 118(19): e2019580118. Published online 2021 May 3. doi: 10.1073/pnas.2019580118
PMCID:
PMC8126796
AbstractArticlePDF–2.4M
19.
Amphiregulin Aggravates Glomerulonephritis via Recruitment and Activation of Myeloid Cells
Simon Melderis, Julia Hagenstein, Matthias Tobias Warkotsch, Julien Dang, Georg Rudolf Herrnstadt, Christoph Benjamin Niehus, Katrin Neumann, Ulf Panzer, Carmen Berasain, Matias A. Avila, Pierre-Louis Tharaux, Gisa Tiegs, Oliver M. Steinmetz
J Am Soc Nephrol. 2020 Sep; 31(9): 1996–2012. Published online 2020 Jul 2. doi: 10.1681/ASN.2019111215
PMCID:
PMC7461677
AbstractArticle
20.
A reference map of the human binary protein interactome
Katja Luck, Dae-Kyum Kim, Luke Lambourne, Kerstin Spirohn, Bridget E. Begg, Wenting Bian, Ruth Brignall, Tiziana Cafarelli, Francisco J. Campos-Laborie, Benoit Charloteaux, Dongsic Choi, Atina G. Coté, Meaghan Daley, Steven Deimling, Alice Desbuleux, Amélie Dricot, Marinella Gebbia, Madeleine F. Hardy, Nishka Kishore, Jennifer J. Knapp, István A. Kovács, Irma Lemmens, Miles W. Mee, Joseph C. Mellor, Carl Pollis, Carles Pons, Aaron D. Richardson, Sadie Schlabach, Bridget Teeking, Anupama Yadav, Mariana Babor, Dawit Balcha, Omer Basha, Christian Bowman-Colin, Suet-Feung Chin, Soon Gang Choi, Claudia Colabella, Georges Coppin, Cassandra D’Amata, David De Ridder, Steffi De Rouck, Miquel Duran-Frigola, Hanane Ennajdaoui, Florian Goebels, Liana Goehring, Anjali Gopal, Ghazal Haddad, Elodie Hatchi, Mohamed Helmy, Yves Jacob, Yoseph Kassa, Serena Landini, Roujia Li, Natascha van Lieshout, Andrew MacWilliams, Dylan Markey, Joseph N. Paulson, Sudharshan Rangarajan, John Rasla, Ashyad Rayhan, Thomas Rolland, Adriana San-Miguel, Yun Shen, Dayag Sheykhkarimli, Gloria M. Sheynkman, Eyal Simonovsky, Murat Taşan, Alexander Tejeda, Vincent Tropepe, Jean-Claude Twizere, Yang Wang, Robert J. Weatheritt, Jochen Weile, Yu Xia, Xinping Yang, Esti Yeger-Lotem, Quan Zhong, Patrick Aloy, Gary D. Bader, Javier De Las Rivas, Suzanne Gaudet, Tong Hao, Janusz Rak, Jan Tavernier, David E. Hill, Marc Vidal, Frederick P. Roth, Michael A. Calderwood
Nature. Author manuscript; available in PMC 2020 Oct 8.
Published in final edited form as: Nature. 2020 Apr; 580(7803): 402–408. Published online 2020 Apr 8. doi: 10.1038/s41586-020-2188-x
PMCID:
PMC7169983
AbstractArticlePDF–5.4M

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