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<article xmlns:xlink="http://www.w3.org/1999/xlink" article-type="research-article" dtd-version="1.1d1">
  <front>
    <journal-meta>
      <journal-title-group>
        <journal-title>Biomedical Research and Therapy</journal-title>
      </journal-title-group>
      <issn pub-type="epub" publication-format="electronic">2198-4093</issn>
      <publisher>
        <publisher-name>BioMedPress</publisher-name>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.7603/s40730-016-0003-y</article-id>
      <article-categories>
        <subj-group subj-group-type="display-channel">
          <subject>Research Article</subject>
        </subj-group>
        <subj-group subj-group-type="heading">
          <subject>Biomedical Research and Therapy</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Significance of Mast cells in Non-neoplastic and Neoplastic lesions of Uterine Cervix</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>R</surname>
            <given-names>Kalyani</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
          <xref ref-type="corresp" rid="cor1">*</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>G</surname>
            <given-names>Rajeshwari</given-names>
          </name>
          <xref ref-type="aff" rid="aff1"/>
        </contrib>
        <aff id="aff1">
          <institution>Department of Pathology, MVJ Medical College &amp; Research Hospital Hosakote, Bangalore, India</institution>
        </aff>
      </contrib-group>
      <author-notes>
        <corresp id="cor1"><label>*</label>For correspondence: <email>drkalyanir@rediffmail.com</email></corresp>
        <fn fn-type="con" id="equal-contrib">
          <label>*</label>
          <p>These authors contributed equally to this work</p>
        </fn>
      </author-notes>
      <pub-date date-type="pub" publication-format="electronic">
        <day>29</day>
        <month>01</month>
        <year>2016</year>
      </pub-date>
      <volume>3</volume>
      <issue>1</issue>
      <fpage>469</fpage>
      <lpage>475</lpage>
      <history>
        <date date-type="received">
          <day>25</day>
          <month>12</month>
          <year>2015</year>
        </date>
        <date date-type="accepted">
          <day>25</day>
          <month>01</month>
          <year>2016</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>Copyright: &#169; The Author(s) 2016</copyright-statement>
        <copyright-year>2016</copyright-year>
        <license license-type="open-access" xlink:href="http://creativecommons.org/licenses/CC-BY/4.0">
          <license-p>This article is distributed under the terms of the Creative Commons Attribution License (CC-BY 4.0) which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.</license-p>
        </license>
      </permissions>
      <abstract>
        <p>Background:</p>
        <p>Mast cells are involved in multiple biological events. The significance of mast cells in non-neoplastic and neoplastic lesions of the cervix has been studied with conflicting results. Its presence in a tumor has been described as evidence of host immunologic antitumor response, angiogenesis and tumor invasion.</p>
        <p>Aims/Objectives:</p>
        <p>To study mast cell density in various cervical lesions using Toluidine blue stain. To compare the sections studied with conventional Toluidine blue staining and Toluidine blue staining by reducing the pH.</p>
        <p>Methodology:</p>
        <p>Cervical biopsy/hysterectomy specimens from archives of the Department of Pathology were considered for the study. The sections were studied for histomorphology and mast cell density. The mast cell density was assessed by Toluidine blue staining by conventional method and another method by reducing pH using weak HCL. The stained slides were reviewed for mast cell density under 10 high power field and statistically analyzed.</p>
        <p>Results:</p>
        <p>Total of 100 cases was studied. Normal cervix 7 cases with the mean age of 44.29 and the mean mast cell density of 45.43. Chronic cervicitis and polypoidal endocervicitis were 26 and 28 cases, the mean age of 45.38 years and 39.14 years and the mean mast cell count of 48.38 and 66.96 respectively. Intraepithelial lesions and malignancy were 23 and 16 cases, the mean age of 43.56 years and 52.26 years and the mean mast cell of 34.47 and 34.6 respectively. The maximum number of mast cells was seen in polypoidal endocervicitis and the least number in squamous cell carcinoma of cervix.</p>
        <p>Conclusion:</p>
        <p>The role of mast cell differs in inflammatory and neoplastic lesions of cervix. Mast cells has an active role in inflammatory lesions.</p>
      </abstract>
      <kwd-group>
        <kwd>Cervix</kwd>
        <kwd>cervicitis</kwd>
        <kwd>cervical intraepithelial neoplasia</kwd>
        <kwd>cervical cancer</kwd>
        <kwd>Toluidine blue</kwd>
      </kwd-group>
    </article-meta>
  </front>
  <body>
    <sec id="s1" sec-type="intro">
      <title>Introduction</title>
      <p>Mast cells were first described by Paul Ehrlich in 1878 as the effect, particularly in the early and acute phases of allergic reactions. It has been only in the past two decades that mast cells have gained recognition for their involvement in other physiological and pathological processes <xref ref-type="bibr" rid="ref4">Mainali et al., 2014</xref>. Mast cells are heterogeneous group of immune cells involved in multiple biological events. They are a component of cancer microenvironment, the role of which is complex and poorly understood. The significance of mast cells in non-neoplastic and neoplastic lesions of cervix has been studied with conflicting results <xref ref-type="bibr" rid="ref3">Gousuddin et al., 2015</xref>.</p>
      <p>The presence of mast cells in tumor has been described as evidence of host immunologic antitumor response and if they are abundant the prognosis is good. However, according to other studies, granules of mast cells are involved in angiogenesis and tumor invasion. Mast cells promote cancer growth by stimulation of neoangiogenesis, tissue remodelling and by modulation of the host immune response <xref ref-type="bibr" rid="ref2">Dyduch et al., 2012</xref>.</p>
      <p>In this study, we tried to demonstrate and compare the presence of mast cell in various neoplastic and nonneoplastic conditions as well as their value as a prognostic indicator with the relationship of mast cell number.</p>
    </sec>
    <sec id="s2" sec-type="materials|methods">
      <title>Materials and Methods</title>
      <p>The study was undertaken in the Department of Pathology at MVJ Medical College Hosakote, Bangalore over a two-year period from June 2013 to June 2015. All the cervical biopsies and hysterectomy specimens received were considered for the study. Relevant clinical information regarding age, parity, clinical features and provisional diagnosis were obtained from the hospital records. The blocks and slides were retrieved from department archives. Hematoxylin and Eosin [H&amp;E] stained slides were reviewed and lesions were categorized as non-neoplastic and neoplastic lesions. Cases with incomplete clinical details and nonavailability of blocks / slides were excluded from the study.</p>
      <p>Non-neoplastic lesions were 61 cases consisting of 7 cases of normal cervix, 26 cases of chronic cervicitis and 28 cases polypoidal endocervicitis. Neoplastic lesions were 39 cases consisting of 16 cases of low grade squamous intraepithelial lesions (LSIL), 6 cases of high grade squamous intraepithelial lesions (HSIL), 1 cases of low grade cervical glandular Intraepithelial Lesion (CGIN), 16 cases of Squamous cell carcinoma (SCC). LSIL included Koilocytic change and Cervical Intraepithelial neoplasia-1 (CIN-1). HSIL included CIN-II and CIN-III <xref ref-type="bibr" rid="ref1">Darragh et al., 2012</xref>. CGIN showed tufting of endocervical lining epithelial cells with increased N:C ratio and without nuclear atypia.</p>
      <p>The blocks were selected; 3-4&#956;m thin sections were cut and stained with Toluidine blue to identify the mast cells with the typical metachromatic granules. Initially 1% Toluidine blue stain was used. Later 1% Toluidine blue stain of pH 4.5 was used which showed better visualization of mast cells.</p>
      <p>The stained slide is first seen under low power to assess the quality of the stain. Mast cells were counted under 40X magnification for 10 consecutive fields in each slide in areas where maximum mast cells were seen and mast cell density (MCD) was calculated. Mast cell density of different histomorphological group were compared and analyzed by Analysis of Variance (ANOVA) statistical method. The sections of conventional Toluidine blue staining and Toluidine blue staining by reducing the pH are also compared.</p>
    </sec>
    <sec id="s3" sec-type="results">
      <title>Results</title>
      <p>Total of 100 cases were included in this study which comprised of 61 cases of non-neoplastic lesions (Normal cervix - 7, chronic cervicitis - 26 and polypoidal endocervicitis - 28cases) and 39 cases of neoplastic lesions (LSIL-16, HSIL-6, CGIN-1, SCC-16 cases). The age distribution in various non-neoplastic and neoplastic lesions is shown in <xref ref-type="fig" rid="tab1"> Table 1 </xref> . Age distribution and mast cell count of various non-neoplastic and neoplastic lesions are shown in <xref ref-type="fig" rid="tab2"> Table 2 </xref> and <xref ref-type="fig" rid="tab3"> Table 3 </xref> respectively.</p>
      <fig id="tab1">
        <label>Table 1</label>
        <caption>
          <p>Age distribution in various cervical lesions</p>
        </caption>
        <graphic xlink:href="s40730-016-0003-y/tab1.png"/>
      </fig>
      <fig id="tab2">
        <label>Table 2</label>
        <caption>
          <p>Comparison of age distribution and mast cell count in various non-neoplastic cervical lesions</p>
        </caption>
        <graphic xlink:href="s40730-016-0003-y/tab2.png"/>
      </fig>
      <fig id="tab3">
        <label>Table 3</label>
        <caption>
          <p>Comparison of age distribution and mast cell count in various cervical neoplastic lesions</p>
        </caption>
        <graphic xlink:href="s40730-016-0003-y/tab3.png"/>
      </fig>
      <p>P value of &lt;0.05 was considered significant. The age distribution in non-neoplastic lesions were not statistically significant (P value 0.087), however it was significant in neoplastic lesions (P value 0.02) as the age difference between LSIL/HSIL to cervical cancer was 10 years. Mast cell counts in non-neoplastic lesions were statistically significant (P value 0.008), as mast cells were maximum in polypoidal endocervicitis. In neoplastic lesions it was not statistically significant (P value 0.349). However, the count was low in SCC compared to LSIL and HSIL.</p>
    </sec>
    <sec id="s4" sec-type="discussion">
      <title>Discussion</title>
      <p>Mast cells are developed in the bone marrow and mature under local tissue microenvironment in the tissues. Mast cells are normally present around the blood vessels, skin, gastrointestinal tract and lungs, sites where it is exposed to foreign /external agents. Mast cells act as a first defense against invasion by outside agents <xref ref-type="bibr" rid="ref7">Theoharides and Cochrane, 2004</xref>.</p>
      <sec id="s4-1">
        <title>Role of mast cells in inflammation</title>
        <p>Mast cells play an important role in various allergic and inflammatory conditions. Mast cells have membrane bound granules that contain a variety of biologically active mediators like histamine, proteoglycans, leukotriene (LT C4, D4, and B4), prostaglandin D2 and Platelet activating factor (PAF). These mediators cause vasodilatation, increased vascular permeability, smooth muscle spasm and cellular infiltration with inflammatory cells <xref ref-type="bibr" rid="ref2">Dyduch et al., 2012</xref>.</p>
      </sec>
      <sec id="s4-2">
        <title>Role of mast cells in neoplasia</title>
        <p>Mast cells also play an important role in tumor progression, the role of which is complex and poorly understood. Mast cells promote cancer growth by modulation of cancer microenvironment which includes fibroblasts, myofibroblasts, newly formed blood vessels and inflammatory cells. Mast cells act in cancer microenvironment as both promoter and inhibitor of tumor growth <xref ref-type="bibr" rid="ref2">Dyduch et al., 2012</xref>.</p>
      </sec>
      <sec id="s4-3">
        <title>Mast cells as tumor promoters</title>
        <p>Mast cells release proangiogenic and mitogenic factors and are involved in the degradation of the extracellular matrix. Histamine released by mast cells induces tumor proliferation through H1 receptors and suppress the immune system through H2 receptors and Interleukin-10 (IL-10), and tumor necrosis &#945; (TNF-&#945;). Mast cells also release proangiogenic factors such as vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), transforming growth factor-&#946; (TGF-&#946;), IL-8 and matrix metalloproteinases which are involved in extracellular matrix degradation. Mast cells release chemical mediators that cause vasodilatation, edema with protein rich exudate. Perhaps such a milieu favours tumor invasion and spread.</p>
      </sec>
      <sec id="s4-4">
        <title>Mast cells in inhibition of tumor growth</title>
        <p>The antineoplastic actions include direct inhibition of cell growth, increased inflammatory activity, induction of apoptosis and decreased cell mobility. Mediators released by the mast cells i.e. TNF-&#945;, IL-1 and IL-6 have inhibitory effect on tumor growth and angiogenesis <xref ref-type="bibr" rid="ref2">Dyduch et al., 2012</xref>.</p>
        <p>In the present study mast cells were mainly present in the areas of inflammation, sub-epithelial stroma and around dilated endocervical glands. In the present study, age distribution was not statistically significant in non-neoplastic lesions; however, it was significant in neoplastic lesions. The observation of our study showed that the age in cervical cancer was 10 years more than that of cervical intraepithelial lesions. These findings were similar to other studies in the past as shown in <xref ref-type="fig" rid="tab6"> Table 6 </xref> . The results of the present study are correlating with other studies. A ten-year interval is very well evident between cervical dysplasia and carcinoma.</p>
        <fig id="tab6">
          <label>Table 6</label>
          <caption>
            <p>Shows mean age in non-neoplastic and neoplastic lesions of cervix in various studies</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/tab6.png"/>
        </fig>
        <p>A study done by Mainali et al showed that mean mast cell count was more in polypoidal endocervicitis which was similar to the present study as shown in <xref ref-type="fig" rid="tab7"> Table 7 </xref> . The mast cell count was significant in nonneoplastic lesions. Majeed SK studied distribution of mast cells in various organs of mice and showed that there is increased number of mast cells in the inflammatory lesions. Jain PC et al showed an increase of mast cells in inflammatory processes <xref ref-type="bibr" rid="ref5">Majeed, 1994</xref>. In our study also there is a well-established relationship in non-neoplastic lesions of uterine cervix with the mast cell count being more in polypoidal endocervicitis (<xref ref-type="fig" rid="tab7"> Table 7 </xref>).</p>
        <fig id="tab7">
          <label>Table 7</label>
          <caption>
            <p>Shows the mast cells in non-neoplastic and neoplastic lesions of cervix</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/tab7.png"/>
        </fig>
        <p>The statistical study showed no correlation with reference to mast cells in neoplastic lesions. However, among the neoplastic lesions least mast cell count was seen in SCC (<xref ref-type="fig" rid="tab3"> Table 3 </xref>).</p>
        <p><xref ref-type="fig" rid="tab7"> Table 7 </xref> shows the mast cell count in non-neoplastic and neoplastic lesions of cervix. Some studies have shown maximum in chronic cervicitis compared to polypoidal endocervicitis. However, in other studies maximum count was seen in polypoidal endocervicitis compared to chronic cervicitis as in our study (Mainali et al). Comparing the mast cell count between nonneoplastic and neoplastic lesions in various studies it was observed that the count was decreased in neoplastic lesions of cervix as in our study. Comparing the mast cell count in cervical dysplasia and carcinoma cervix,some studies showed increase in mast cell count in carcinoma cervix compared to cervical dysplasia, in other studies the count is more in cervical dysplasia compared to carcinoma cervix as in the present study <xref ref-type="bibr" rid="ref3">Gousuddin et al., 2015</xref>. Mean mast cell count was more in non-neoplastic lesions and least in SCC of cervix.</p>
        <p>However, in one of study they showed that there is no correlation between the mast cells and age of the patient (<xref ref-type="fig" rid="tab4"> Table 4 </xref>). There is inverse relation between mast cell count and degree of dysplasia <xref ref-type="bibr" rid="ref6">Sridharan and Shankar, 2012</xref> and probably related to decrease in immunity with advancing age (<xref ref-type="fig" rid="tab5"> Table 5 </xref>).</p>
        <fig id="tab4">
          <label>Table 4</label>
          <caption>
            <p>Relation between Age range and mean mast cell count</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/tab4.png"/>
        </fig>
        <fig id="tab5">
          <label>Table 5</label>
          <caption>
            <p>Shows that as age advances the average mast cell count decreased</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/tab5.png"/>
        </fig>
        <p>The observation of progressively decreasing mast cell counts from mild to severe dysplasia and invasive carcinomas, suggests that mast cell count appears inversely proportional to the degree of dysplasia.</p>
        <p>
          <xref ref-type="fig" rid="fig1"> Figure 1 </xref>
          <fig id="fig1">
            <label>Figure 1</label>
            <caption>
              <title>Chronic cervicitis</title>
              <p>a.H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
            </caption>
            <graphic xlink:href="s40730-016-0003-y/fig1.png"/>
          </fig>
          <xref ref-type="fig" rid="fig2"> Figure 2 </xref>
          <fig id="fig2">
            <label>Figure 2</label>
            <caption>
              <title>Polypoidal endocervicitis</title>
              <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
            </caption>
            <graphic xlink:href="s40730-016-0003-y/fig2.png"/>
          </fig>
          <xref ref-type="fig" rid="fig3"> Figure 3 </xref>
          <fig id="fig3">
            <label>Figure 3</label>
            <caption>
              <title>LSIL</title>
              <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
            </caption>
            <graphic xlink:href="s40730-016-0003-y/fig3.png"/>
          </fig>
          <xref ref-type="fig" rid="fig4"> Figure 4 </xref>
          <fig id="fig4">
            <label>Figure 4</label>
            <caption>
              <title>HSIL</title>
              <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
            </caption>
            <graphic xlink:href="s40730-016-0003-y/fig4.png"/>
          </fig>
          <xref ref-type="fig" rid="fig5"> Figure 5 </xref>
          <fig id="fig5">
            <label>Figure 5</label>
            <caption>
              <title>SCC</title>
              <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
            </caption>
            <graphic xlink:href="s40730-016-0003-y/fig5.png"/>
          </fig>
          <xref ref-type="fig" rid="fig6"> Figure 6 </xref>
          <fig id="fig6">
            <label>Figure 6</label>
            <caption>
              <title>CGIN</title>
              <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
            </caption>
            <graphic xlink:href="s40730-016-0003-y/fig6.png"/>
          </fig>
        </p>
        <fig id="fig1">
          <label>Figure 1</label>
          <caption>
            <title>Chronic cervicitis</title>
            <p>a.H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/fig1.png"/>
        </fig>
        <fig id="fig2">
          <label>Figure 2</label>
          <caption>
            <title>Polypoidal endocervicitis</title>
            <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/fig2.png"/>
        </fig>
        <fig id="fig3">
          <label>Figure 3</label>
          <caption>
            <title>LSIL</title>
            <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/fig3.png"/>
        </fig>
        <fig id="fig4">
          <label>Figure 4</label>
          <caption>
            <title>HSIL</title>
            <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/fig4.png"/>
        </fig>
        <fig id="fig5">
          <label>Figure 5</label>
          <caption>
            <title>SCC</title>
            <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/fig5.png"/>
        </fig>
        <fig id="fig6">
          <label>Figure 6</label>
          <caption>
            <title>CGIN</title>
            <p>a. H &amp; E (x100), b. Toluidine blue (x400), c. Toluidine blue pH 4.5 (x400).</p>
          </caption>
          <graphic xlink:href="s40730-016-0003-y/fig6.png"/>
        </fig>
      </sec>
    </sec>
    <sec id="s5" sec-type="conclusion">
      <title>Conclusion</title>
      <p>Mast cells are increased in inflammatory lesions of cervix with maximum in polypoidal endocervicitis and least in SCC of cervix. There is statistical significant correlation with reference to mast cells in non &#8211; neoplastic lesions and it was not statistically significant with reference to age. In neoplastic lesions statistical significant correlation was observed with reference to age but it no statistical correlation was observed with reference to mast cells.The role of mast cell differs in inflammatory and neoplastic lesions of cervix; indicating active role in inflammatory lesions.</p>
    </sec>
  </body>
  <back>
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