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Prognostic Impact of Melatonin Receptors MT1 and MT2 in Non-Small Cell Lung Cancer (NSCLC)
: Several studies have investigated the inhibitory effect of melatonin on lung cancer cells. There are no data available on the prognostic impact of melatonin receptors MT1 and MT2 in non-small cell lung cancer (NSCLC). : Immunohistochemical studies of MT1 and MT2 were conducted on NSCLC (N = 786) a...
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Published in: | Cancers 2019-07, Vol.11 (7), p.1001 |
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creator | Jablonska, Karolina Nowinska, Katarzyna Piotrowska, Aleksandra Partynska, Aleksandra Katnik, Ewa Pawelczyk, Konrad Glatzel-Plucinska, Natalia Podhorska-Okolow, Marzenna Dziegiel, Piotr |
description | : Several studies have investigated the inhibitory effect of melatonin on lung cancer cells. There are no data available on the prognostic impact of melatonin receptors MT1 and MT2 in non-small cell lung cancer (NSCLC).
: Immunohistochemical studies of MT1 and MT2 were conducted on NSCLC (N = 786) and non-malignant lung tissue (NMLT) (N = 120) using tissue microarrays. Molecular studies were performed on frozen fragments of NSCLC (N = 62; real time PCR), NMLT (N = 24) and lung cancer cell lines NCI-H1703, A549 and IMR-90 (real time PCR, western blot).
: The expression of both receptors was higher in NSCLC than in NMLT. Higher MT1 and MT2 expression levels (at protein and mRNA) were noted in squamous cell carcinomas (SCC) compared to adenocarcinomas (AC). MT1 immunoexpression decreased as both the tumour size and the cancer stage increased in the whole cohort, while MT2 decreased as the cancer stage increased, with lymph node involvement (in the whole study group) and increasing malignancy grade (in SCC). Higher expression of MT2 was associated with a favorable prognosis. MT2 was an independent prognostic factor for overall survival (OS) in all analyzed NSCLC and in smoking patients.
: Our observations may point to the potential prognostic significance of MT2 in NSCLC. |
doi_str_mv | 10.3390/cancers11071001 |
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: Immunohistochemical studies of MT1 and MT2 were conducted on NSCLC (N = 786) and non-malignant lung tissue (NMLT) (N = 120) using tissue microarrays. Molecular studies were performed on frozen fragments of NSCLC (N = 62; real time PCR), NMLT (N = 24) and lung cancer cell lines NCI-H1703, A549 and IMR-90 (real time PCR, western blot).
: The expression of both receptors was higher in NSCLC than in NMLT. Higher MT1 and MT2 expression levels (at protein and mRNA) were noted in squamous cell carcinomas (SCC) compared to adenocarcinomas (AC). MT1 immunoexpression decreased as both the tumour size and the cancer stage increased in the whole cohort, while MT2 decreased as the cancer stage increased, with lymph node involvement (in the whole study group) and increasing malignancy grade (in SCC). Higher expression of MT2 was associated with a favorable prognosis. MT2 was an independent prognostic factor for overall survival (OS) in all analyzed NSCLC and in smoking patients.
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: Immunohistochemical studies of MT1 and MT2 were conducted on NSCLC (N = 786) and non-malignant lung tissue (NMLT) (N = 120) using tissue microarrays. Molecular studies were performed on frozen fragments of NSCLC (N = 62; real time PCR), NMLT (N = 24) and lung cancer cell lines NCI-H1703, A549 and IMR-90 (real time PCR, western blot).
: The expression of both receptors was higher in NSCLC than in NMLT. Higher MT1 and MT2 expression levels (at protein and mRNA) were noted in squamous cell carcinomas (SCC) compared to adenocarcinomas (AC). MT1 immunoexpression decreased as both the tumour size and the cancer stage increased in the whole cohort, while MT2 decreased as the cancer stage increased, with lymph node involvement (in the whole study group) and increasing malignancy grade (in SCC). Higher expression of MT2 was associated with a favorable prognosis. MT2 was an independent prognostic factor for overall survival (OS) in all analyzed NSCLC and in smoking patients.
: Our observations may point to the potential prognostic significance of MT2 in NSCLC.</description><subject>Breast cancer</subject><subject>Cancer therapies</subject><subject>Chemotherapy</subject><subject>Kinases</subject><subject>Lung cancer</subject><subject>Lymph nodes</subject><subject>Malignancy</subject><subject>Melatonin</subject><subject>Melatonin receptors</subject><subject>Metastasis</subject><subject>mRNA</subject><subject>Mutation</subject><subject>Non-small cell lung carcinoma</subject><subject>Phosphorylation</subject><subject>Proteins</subject><subject>Radiation</subject><subject>Small cell lung carcinoma</subject><subject>Smoking</subject><subject>Squamous cell carcinoma</subject><subject>Transcription factors</subject><subject>Tumor cell lines</subject><subject>Tumors</subject><issn>2072-6694</issn><issn>2072-6694</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkUtLJDEUhYMo06KuZyeB2eiixrw6qWwEKdQR2gfTvZpNSOfRU1KVtEmV4L83o07Tehe5gfvdwz0cAL5j9JNSic6MDsaljDESGCG8A_YJEqTiXLLdrf8EHOX8iEpRigUX38CEYoolR2If_HlIcRViHloDb_q1NgOMHt66Tg8xtAH-dsath5gyvF1gqIMtncAyuIuhmve662DjyjMbwwo2bwfBk7t5M2tOD8Ge1112Rx_9ACyuLhfNr2p2f33TXMwqwwgeKo-oYIxwK5cG1bz2lNEasZoxhrhxU-u8WHpkuZFkaizH0mHtuWfWSSstPQDn77Lrcdk7a1wYku7UOrW9Ti8q6lZ9noT2r1rFZ8W5kBjVReDkQyDFp9HlQfVtNsWUDi6OWRHCMWGU1qygP76gj3FMobhTZMoEk0QgUaizd8qkmHNyfnMMRupfcupLcmXjeNvDhv-fE30FbRGTYA</recordid><startdate>20190717</startdate><enddate>20190717</enddate><creator>Jablonska, Karolina</creator><creator>Nowinska, Katarzyna</creator><creator>Piotrowska, Aleksandra</creator><creator>Partynska, Aleksandra</creator><creator>Katnik, Ewa</creator><creator>Pawelczyk, Konrad</creator><creator>Glatzel-Plucinska, Natalia</creator><creator>Podhorska-Okolow, Marzenna</creator><creator>Dziegiel, Piotr</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7T5</scope><scope>7TO</scope><scope>7XB</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8292-1385</orcidid><orcidid>https://orcid.org/0000-0003-4093-7386</orcidid><orcidid>https://orcid.org/0000-0002-4618-9668</orcidid><orcidid>https://orcid.org/0000-0001-8275-7266</orcidid><orcidid>https://orcid.org/0000-0002-6498-717X</orcidid><orcidid>https://orcid.org/0000-0001-6901-1240</orcidid><orcidid>https://orcid.org/0000-0002-7989-3264</orcidid><orcidid>https://orcid.org/0000-0001-8316-8893</orcidid><orcidid>https://orcid.org/0000-0002-7532-0397</orcidid><orcidid>https://orcid.org/0000-0003-2215-5997</orcidid></search><sort><creationdate>20190717</creationdate><title>Prognostic Impact of Melatonin Receptors MT1 and MT2 in Non-Small Cell Lung Cancer (NSCLC)</title><author>Jablonska, Karolina ; Nowinska, Katarzyna ; Piotrowska, Aleksandra ; Partynska, Aleksandra ; Katnik, Ewa ; Pawelczyk, Konrad ; Glatzel-Plucinska, Natalia ; Podhorska-Okolow, Marzenna ; Dziegiel, Piotr</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c421t-f0374426d9bc0868f343804844406ce5def7bf0d6c925cd619e1af6f4de9d9d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Breast cancer</topic><topic>Cancer therapies</topic><topic>Chemotherapy</topic><topic>Kinases</topic><topic>Lung cancer</topic><topic>Lymph nodes</topic><topic>Malignancy</topic><topic>Melatonin</topic><topic>Melatonin receptors</topic><topic>Metastasis</topic><topic>mRNA</topic><topic>Mutation</topic><topic>Non-small cell lung carcinoma</topic><topic>Phosphorylation</topic><topic>Proteins</topic><topic>Radiation</topic><topic>Small cell lung carcinoma</topic><topic>Smoking</topic><topic>Squamous cell carcinoma</topic><topic>Transcription factors</topic><topic>Tumor cell lines</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jablonska, Karolina</creatorcontrib><creatorcontrib>Nowinska, Katarzyna</creatorcontrib><creatorcontrib>Piotrowska, Aleksandra</creatorcontrib><creatorcontrib>Partynska, Aleksandra</creatorcontrib><creatorcontrib>Katnik, Ewa</creatorcontrib><creatorcontrib>Pawelczyk, Konrad</creatorcontrib><creatorcontrib>Glatzel-Plucinska, Natalia</creatorcontrib><creatorcontrib>Podhorska-Okolow, Marzenna</creatorcontrib><creatorcontrib>Dziegiel, Piotr</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection (Proquest) (PQ_SDU_P3)</collection><collection>Biological Sciences</collection><collection>ProQuest research library</collection><collection>ProQuest Biological Science Journals</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jablonska, Karolina</au><au>Nowinska, Katarzyna</au><au>Piotrowska, Aleksandra</au><au>Partynska, Aleksandra</au><au>Katnik, Ewa</au><au>Pawelczyk, Konrad</au><au>Glatzel-Plucinska, Natalia</au><au>Podhorska-Okolow, Marzenna</au><au>Dziegiel, Piotr</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic Impact of Melatonin Receptors MT1 and MT2 in Non-Small Cell Lung Cancer (NSCLC)</atitle><jtitle>Cancers</jtitle><addtitle>Cancers (Basel)</addtitle><date>2019-07-17</date><risdate>2019</risdate><volume>11</volume><issue>7</issue><spage>1001</spage><pages>1001-</pages><issn>2072-6694</issn><eissn>2072-6694</eissn><abstract>: Several studies have investigated the inhibitory effect of melatonin on lung cancer cells. There are no data available on the prognostic impact of melatonin receptors MT1 and MT2 in non-small cell lung cancer (NSCLC).
: Immunohistochemical studies of MT1 and MT2 were conducted on NSCLC (N = 786) and non-malignant lung tissue (NMLT) (N = 120) using tissue microarrays. Molecular studies were performed on frozen fragments of NSCLC (N = 62; real time PCR), NMLT (N = 24) and lung cancer cell lines NCI-H1703, A549 and IMR-90 (real time PCR, western blot).
: The expression of both receptors was higher in NSCLC than in NMLT. Higher MT1 and MT2 expression levels (at protein and mRNA) were noted in squamous cell carcinomas (SCC) compared to adenocarcinomas (AC). MT1 immunoexpression decreased as both the tumour size and the cancer stage increased in the whole cohort, while MT2 decreased as the cancer stage increased, with lymph node involvement (in the whole study group) and increasing malignancy grade (in SCC). Higher expression of MT2 was associated with a favorable prognosis. MT2 was an independent prognostic factor for overall survival (OS) in all analyzed NSCLC and in smoking patients.
: Our observations may point to the potential prognostic significance of MT2 in NSCLC.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>31319607</pmid><doi>10.3390/cancers11071001</doi><orcidid>https://orcid.org/0000-0002-8292-1385</orcidid><orcidid>https://orcid.org/0000-0003-4093-7386</orcidid><orcidid>https://orcid.org/0000-0002-4618-9668</orcidid><orcidid>https://orcid.org/0000-0001-8275-7266</orcidid><orcidid>https://orcid.org/0000-0002-6498-717X</orcidid><orcidid>https://orcid.org/0000-0001-6901-1240</orcidid><orcidid>https://orcid.org/0000-0002-7989-3264</orcidid><orcidid>https://orcid.org/0000-0001-8316-8893</orcidid><orcidid>https://orcid.org/0000-0002-7532-0397</orcidid><orcidid>https://orcid.org/0000-0003-2215-5997</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Breast cancer Cancer therapies Chemotherapy Kinases Lung cancer Lymph nodes Malignancy Melatonin Melatonin receptors Metastasis mRNA Mutation Non-small cell lung carcinoma Phosphorylation Proteins Radiation Small cell lung carcinoma Smoking Squamous cell carcinoma Transcription factors Tumor cell lines Tumors |
title | Prognostic Impact of Melatonin Receptors MT1 and MT2 in Non-Small Cell Lung Cancer (NSCLC) |
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