Here's how LINK.SPRINGER.COM makes money* and how much!

*Please read our disclaimer before using our estimates.
Loading...

LINK . SPRINGER . COM {}

  1. Analyzed Page
  2. Matching Content Categories
  3. CMS
  4. Monthly Traffic Estimate
  5. How Does Link.springer.com Make Money
  6. Keywords
  7. Topics
  8. Schema
  9. External Links
  10. Analytics And Tracking
  11. Libraries
  12. CDN Services

We are analyzing https://link.springer.com/article/10.1007/bf01980969.

Title:
Multiple growth factor independence in rat mammary carcinoma cells | Breast Cancer Research and Treatment
Description:
In previous studies we demonstrated that rat mammary tumor (RMT) cells that are serially transplantable consist of cells that are independent of growth factors strictly required by normal rat mammary epithelial (RME) cells for growth in serum-free culture. The present studies were designed to determine the extent of the growth factor independence of several cell lines derived from these tumors and to determine if the cells that expressed growth factor independencein vitro are also tumorigenicin vivo. Cells from a transplantable mammary carcinoma (8–12 RMT) were seeded into culture in serum-free medium in the absence of either insulin (IN), epidermal growth factor (EGF), or cholera toxin (CT), and cell populations independent of the individual factors were developed. Next, the three growth factor independent populations were tested for their ability to grow in the absence of multiple growth factors. 8–12 RMT cells did not lose proliferative potential when multiple growth factors were deleted from the medium. Indeed, 8–12 RMT cells could be serially propagated in serum-free medium supplemented solely with bovine serum albumin (BSA) and ethanolamine. Cell lines independent of single growth factors were also developed from two other transplantable tumors (1–9 RMT and 7–15 RMT). In contrast to the 8–12 RMT-derived cell lines, deletion of additional growth factors from the media of the 1–9 RMT and 7–15 RMT-derived cells resulted in dramatic losses in growth potential. These results suggest that independence of individual growth factors is mediated by different mechanisms, since cells from different tumors can stably express independence of one, two, or three or more factors. Examination of conditioned media of four different RMT cell lines indicates that independence of EGF is mediated by autocrine factors. By contrast, there is no evidence for an autocrine factor that mediates independence of insulin-like growth factors. Thus, cell lines derived from serially transplantable RMTs are independent of either single or multiple growth factors, and independence of individual growth factors appears to be mediated by separate mechanisms.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Science
  • Education
  • Family & Parenting

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 8,123,328 visitors per month in the current month.

check SE Ranking
check Ahrefs
check Similarweb
check Ubersuggest
check Semrush

How Does Link.springer.com Make Money? {πŸ’Έ}

We don’t know how the website earns money.

Some websites aren't about earning revenue; they're built to connect communities or raise awareness. There are numerous motivations behind creating websites. This might be one of them. Link.springer.com might be earning cash quietly, but we haven't detected the monetization method.

Keywords {πŸ”}

growth, cell, google, scholar, pubmed, factors, article, factor, cells, mammary, independence, cancer, rat, rmt, autocrine, ethier, epithelial, res, serumfree, lines, line, privacy, cookies, content, research, multiple, carcinoma, independent, vitro, medium, potential, access, nature, human, publish, search, breast, transplantable, normal, culture, tumors, epidermal, mediated, synthesis, media, data, information, log, journal, moorthy,

Topics {βœ’οΈ}

cholera toxin rat mammary tumor month download article/chapter epidermal growth factor mda-mb-231 cells embedded autocrine growth factor growth factor independence transplantable mammary carcinoma related subjects serum-free culture conditions growth factor interactions growth factor ii mouse epidermal keratinocytes autocrine growth factors growth factor synthesis full article pdf multiple growth factors privacy choices/manage cookies cell lines derived additional growth factors individual growth factors peptide growth factors exogenous growth factors extended growth potential stably express independence autocrine factor check access instant access serum-free medium single growth factors cell lines independent article ethier growth factor stem cell endothelial cell movement cell populations independent serum-free culture bovine serum albumin mouse 3t3 cells rmt cell lines conditions privacy policy european economic area cyclic amp derivatives michigan medical school lose proliferative potential plasminogen activator synthesis serially transplantable consist serially transplantable rmts myeloid leukemia insulin/insulin

Schema {πŸ—ΊοΈ}

WebPage:
      mainEntity:
         headline:Multiple growth factor independence in rat mammary carcinoma cells
         description:In previous studies we demonstrated that rat mammary tumor (RMT) cells that are serially transplantable consist of cells that are independent of growth factors strictly required by normal rat mammary epithelial (RME) cells for growth in serum-free culture. The present studies were designed to determine the extent of the growth factor independence of several cell lines derived from these tumors and to determine if the cells that expressed growth factor independencein vitro are also tumorigenicin vivo. Cells from a transplantable mammary carcinoma (8–12 RMT) were seeded into culture in serum-free medium in the absence of either insulin (IN), epidermal growth factor (EGF), or cholera toxin (CT), and cell populations independent of the individual factors were developed. Next, the three growth factor independent populations were tested for their ability to grow in the absence of multiple growth factors. 8–12 RMT cells did not lose proliferative potential when multiple growth factors were deleted from the medium. Indeed, 8–12 RMT cells could be serially propagated in serum-free medium supplemented solely with bovine serum albumin (BSA) and ethanolamine. Cell lines independent of single growth factors were also developed from two other transplantable tumors (1–9 RMT and 7–15 RMT). In contrast to the 8–12 RMT-derived cell lines, deletion of additional growth factors from the media of the 1–9 RMT and 7–15 RMT-derived cells resulted in dramatic losses in growth potential. These results suggest that independence of individual growth factors is mediated by different mechanisms, since cells from different tumors can stably express independence of one, two, or three or more factors. Examination of conditioned media of four different RMT cell lines indicates that independence of EGF is mediated by autocrine factors. By contrast, there is no evidence for an autocrine factor that mediates independence of insulin-like growth factors. Thus, cell lines derived from serially transplantable RMTs are independent of either single or multiple growth factors, and independence of individual growth factors appears to be mediated by separate mechanisms.
         datePublished:
         dateModified:
         pageStart:73
         pageEnd:81
         sameAs:https://doi.org/10.1007/BF01980969
         keywords:
            autocrine factors
            cholera toxin
            epidermal growth factor
            growth factor independence
            insulin
            rat mammary tumors
            Oncology
         image:
         isPartOf:
            name:Breast Cancer Research and Treatment
            issn:
               1573-7217
               0167-6806
            volumeNumber:18
            type:
               Periodical
               PublicationVolume
         publisher:
            name:Kluwer Academic Publishers
            logo:
               url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
               type:ImageObject
            type:Organization
         author:
               name:Stephen P. Ethier
               affiliation:
                     name:The University of Michigan Medical School
                     address:
                        name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
                        type:PostalAddress
                     type:Organization
               type:Person
               name:Ramesh Moorthy
               affiliation:
                     name:The University of Michigan Medical School
                     address:
                        name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
                        type:PostalAddress
                     type:Organization
               type:Person
         isAccessibleForFree:
         hasPart:
            isAccessibleForFree:
            cssSelector:.main-content
            type:WebPageElement
         type:ScholarlyArticle
      context:https://schema.org
ScholarlyArticle:
      headline:Multiple growth factor independence in rat mammary carcinoma cells
      description:In previous studies we demonstrated that rat mammary tumor (RMT) cells that are serially transplantable consist of cells that are independent of growth factors strictly required by normal rat mammary epithelial (RME) cells for growth in serum-free culture. The present studies were designed to determine the extent of the growth factor independence of several cell lines derived from these tumors and to determine if the cells that expressed growth factor independencein vitro are also tumorigenicin vivo. Cells from a transplantable mammary carcinoma (8–12 RMT) were seeded into culture in serum-free medium in the absence of either insulin (IN), epidermal growth factor (EGF), or cholera toxin (CT), and cell populations independent of the individual factors were developed. Next, the three growth factor independent populations were tested for their ability to grow in the absence of multiple growth factors. 8–12 RMT cells did not lose proliferative potential when multiple growth factors were deleted from the medium. Indeed, 8–12 RMT cells could be serially propagated in serum-free medium supplemented solely with bovine serum albumin (BSA) and ethanolamine. Cell lines independent of single growth factors were also developed from two other transplantable tumors (1–9 RMT and 7–15 RMT). In contrast to the 8–12 RMT-derived cell lines, deletion of additional growth factors from the media of the 1–9 RMT and 7–15 RMT-derived cells resulted in dramatic losses in growth potential. These results suggest that independence of individual growth factors is mediated by different mechanisms, since cells from different tumors can stably express independence of one, two, or three or more factors. Examination of conditioned media of four different RMT cell lines indicates that independence of EGF is mediated by autocrine factors. By contrast, there is no evidence for an autocrine factor that mediates independence of insulin-like growth factors. Thus, cell lines derived from serially transplantable RMTs are independent of either single or multiple growth factors, and independence of individual growth factors appears to be mediated by separate mechanisms.
      datePublished:
      dateModified:
      pageStart:73
      pageEnd:81
      sameAs:https://doi.org/10.1007/BF01980969
      keywords:
         autocrine factors
         cholera toxin
         epidermal growth factor
         growth factor independence
         insulin
         rat mammary tumors
         Oncology
      image:
      isPartOf:
         name:Breast Cancer Research and Treatment
         issn:
            1573-7217
            0167-6806
         volumeNumber:18
         type:
            Periodical
            PublicationVolume
      publisher:
         name:Kluwer Academic Publishers
         logo:
            url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
            type:ImageObject
         type:Organization
      author:
            name:Stephen P. Ethier
            affiliation:
                  name:The University of Michigan Medical School
                  address:
                     name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
                     type:PostalAddress
                  type:Organization
            type:Person
            name:Ramesh Moorthy
            affiliation:
                  name:The University of Michigan Medical School
                  address:
                     name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
                     type:PostalAddress
                  type:Organization
            type:Person
      isAccessibleForFree:
      hasPart:
         isAccessibleForFree:
         cssSelector:.main-content
         type:WebPageElement
["Periodical","PublicationVolume"]:
      name:Breast Cancer Research and Treatment
      issn:
         1573-7217
         0167-6806
      volumeNumber:18
Organization:
      name:Kluwer Academic Publishers
      logo:
         url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
         type:ImageObject
      name:The University of Michigan Medical School
      address:
         name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
         type:PostalAddress
      name:The University of Michigan Medical School
      address:
         name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
         type:PostalAddress
ImageObject:
      url:https://www.springernature.com/app-sn/public/images/logo-springernature.png
Person:
      name:Stephen P. Ethier
      affiliation:
            name:The University of Michigan Medical School
            address:
               name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
               type:PostalAddress
            type:Organization
      name:Ramesh Moorthy
      affiliation:
            name:The University of Michigan Medical School
            address:
               name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
               type:PostalAddress
            type:Organization
PostalAddress:
      name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
      name:Department of Radiation Oncology, The University of Michigan Medical School, Ann Arbor, USA
WebPageElement:
      isAccessibleForFree:
      cssSelector:.main-content

External Links {πŸ”—}(89)

Analytics and Tracking {πŸ“Š}

  • Google Tag Manager

Libraries {πŸ“š}

  • Clipboard.js
  • Prism.js

CDN Services {πŸ“¦}

  • Crossref

4.45s.