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4 protocols using p130cas

1

Protein Phosphorylation Analysis in Lung Cancer

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Western blotting was performed to assess protein phosphorylation and expression levels in lung cancer cells treated with AC-93253 iodide as described previously [20 (link)]. The EGFR, STAT3 (F-2), PI3K, phospho-MEK1/2 (Ser 218/Ser 222), MEK, phospho-ERK (Tyr204), ERK, Paxillin, and p130cas were purchased from Santa Cruz Biotechnology, Inc. (Dallas, TX, USA). Phospho-Src (pY418), phospho-FAK (Tyr576), and FAK were purchased from Invitrogen (Carlsbad, CA, USA). Phospho-EGFR (Tyr1068), phospho-STAT3 (Tyr 705), phospho-PI3K (Tyr458), phospho-SAPK/Jun N-terminal kinase (JNK) (Thr183/Tyr185), SAPK/JNK, phospho-Paxillin (Tyr118), and phospho-p130cas (Tyr410) were purchased from Cell Signaling Technology (Beverly, MA, USA), and the primary antibody to Src was produced in our laboratory (ATCC CRL-2651). GAPDH (Upstate Biotechnology, Lake Placid, NY, USA) was used as a loading control. The mRNA expression levels of Src and related genes were detected using a real-time PCR machine (ABI prism 7300 Sequence Detection System, Applied Biosystems, Carlsbad, CA, USA) and SYBR Green Reagent (Roche, Basel, Switzerland). TATA-box binding protein (TBP) was used as an internal control (GenBank X54993). Details regarding the procedures and calculations used to perform the experiments are provided elsewhere [21 (link)].
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2

Antibody Validation for Cell Signaling

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The anti-CLEC11A monoclonal antibody (Cat# MAB1904) was purchased from R&D System (Minneapolis, MN, USA). The anti-FAK (Cat# sc-1688), anti-integrins α2 (Cat# sc-6586), α5 (Cat# sc-10729), and β1 (Cat# sc-6622), p130-Cas (Cat# sc-20029), and peroxidase-conjugated secondary antibodies were purchased from Santa Cruz (Santa Cruz, CA, USA). The anti-active integrin β1 antibody (Cat# 550531) was obtained from BD Pharmingen (San Diego, CA, USA). The anti-EGFR (Cat#2232), anti-pEGFR (Y1068, Cat# 2234), anti-pFAK (Y576/577, Cat# 3281), and anti-pp130-Cas (Y165, Cat# 4015) were purchased from Cell Signaling Technology (Beverly, MA, USA). The anti-pFAK (Y397; Cat# ab81298) antibody was purchased from Abcam (Cambridge, UK). The anti-actin (Cat# A5441) was purchased from Sigma-Aldrich (St. Louis, MO, USA). Anti-TGFBI (Cat# GTX100744) and anti-tubulin (Cat# GTX62882) antibodies were obtained from GeneTex (Hsinchu, Taiwan). G418 and Zeocin were purchased from Sigma-Aldrich (St. Louis, MO, USA) and Invitrogen (Carlsbad, CA, USA), respectively. VEGF-A 165 (Cat# 292-VE) and basic FGF (Cat# 234-FSE) were purchased from R&D System (Minneapolis, MN, USA).
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3

Derivation and Characterization of Ovarian Cancer Cell Lines

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MOVCAR cell lines were derived from the ascites of MISIIR-TAg;NEDD9+/+ (MOVCAR-5009, -6111, -7577, -8248, -8250) and MISIIR-TAg;NEDD9−/− (MOVCAR-136, -143, -145, -168) mice in our laboratory as described12 . Human OC cell lines OVCAR-5 and A1847 OC were obtained from the FCCC Cell Culture Facility (deposited by Dr. Thomas Hamilton) and maintained as described56 (link). Cell lines were periodically checked for mycoplasma contamination OVCAR-5 cells were authenticated by STR profiling. Antibodies and commercial source: antibodies recognizing AKT (cat# 468S), pAKTS473 (cat# 3787S), ERK 1/2 (9102), pERK1/2T202-Y204 (cat# 9106S), Src (cat# 2108S), pSrcY416 (cat# 2101S), pSrcY527 (2105S), STAT3 (cat# 9132) and pSTAT3Y705 (cat# 9145S), pan-keratin (cat# 4545) (Cell Signaling Technology; Danvers, MA, USA), NEDD9 (cat# ab18056) (Abcam; Cambridge, MA, USA), SV40-TAg (cat# sc-147), β-actin (cat# sc-8432), E-cadherin (cat# sc-7870), N-cadherin (cat# sc-7939), p130Cas (cat# sc-860) (Santa Cruz Biotechnology; Santa Cruz, CA, USA), BMPR1B (cat# bs-6639R), and FOXJ1 (cat# 36887) (One World Lab; San Diego, CA, USA), and PAX8 (cat# 10336-I-AP) (Proteintech Group, Rosemont, IL, USA).
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4

Derivation and Characterization of Ovarian Cancer Cell Lines

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MOVCAR cell lines were derived from the ascites of MISIIR-TAg;NEDD9+/+ (MOVCAR-5009, -6111, -7577, -8248, -8250) and MISIIR-TAg;NEDD9−/− (MOVCAR-136, -143, -145, -168) mice in our laboratory as described12 . Human OC cell lines OVCAR-5 and A1847 OC were obtained from the FCCC Cell Culture Facility (deposited by Dr. Thomas Hamilton) and maintained as described56 (link). Cell lines were periodically checked for mycoplasma contamination OVCAR-5 cells were authenticated by STR profiling. Antibodies and commercial source: antibodies recognizing AKT (cat# 468S), pAKTS473 (cat# 3787S), ERK 1/2 (9102), pERK1/2T202-Y204 (cat# 9106S), Src (cat# 2108S), pSrcY416 (cat# 2101S), pSrcY527 (2105S), STAT3 (cat# 9132) and pSTAT3Y705 (cat# 9145S), pan-keratin (cat# 4545) (Cell Signaling Technology; Danvers, MA, USA), NEDD9 (cat# ab18056) (Abcam; Cambridge, MA, USA), SV40-TAg (cat# sc-147), β-actin (cat# sc-8432), E-cadherin (cat# sc-7870), N-cadherin (cat# sc-7939), p130Cas (cat# sc-860) (Santa Cruz Biotechnology; Santa Cruz, CA, USA), BMPR1B (cat# bs-6639R), and FOXJ1 (cat# 36887) (One World Lab; San Diego, CA, USA), and PAX8 (cat# 10336-I-AP) (Proteintech Group, Rosemont, IL, USA).
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